510(k) K945832
- Device
- BRADY MEDICAL PRODUCTS TRANSCORBENT AND THINSITE TOPICAL BORDER WOUND DRESSINGS
- Applicant
- BRADY MEDICAL PRODUCTS CO.
- 510(k) number
- K945832
- Product code
- MGQ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1995-03-01
- Date received
- 1994-11-29
- Regulation
- 510(k) Premarket Notification
- Classification name
- Dressing, Wound And Burn, Hydrogel W/drug And/or Biologic
- Medical specialty
- 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
- Review panel
- General & Plastic Surgery
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- DIANE HOCHREIN
- Address
- 727 W. Glendale Ave. P.O. Box 571 Milwaukee WI US 53201 53201
FDA Registration Numbers#
- 3012680643
- 3027617478
- 3007735241
- 3015140210
- 3030017177
- 3027341451
- 3004018264
- 3004799623
- 3015337116
- 3014146451
- 3042251637
- 3012034017
- 1000317571
- 3017210336
- 3013034812
- 3015335956
- 3009548473
- 3015172365
- 1220246
- 3013671177
- 3008258694
- 3045325156
- 3014266447
- 3017896419
- 3011529314
- 3031841433
- 3025413691
- 1038758
- 3014848316
- 3011675351
- 3008255748
- 3003887292
- 3011248038
- 3015168783
- 3012502601
- 3027605322
- 3038284048
- 3016837630
- 3031582449
- 3038356900
- 1423537
- 1219592
- 3015142802
- 3010392991
- 3011247798
- 3005343641
- 3015745029
- 3021282544
- 3027517726
- 3012084379
- 3016170587
- 3015821396
- 3007841320
- 3010814025
- 3013524663
- 3008562678
- 3015142721
- 3032911850
- 3008384335
- 3026331889
- 3011210302
- 3014897003
- 3006611176
- 9616679
- 3018101380
- 3007028032
- 3008808560
- 3007417776
- 3013530949
- 3010952189
- 3010872396
- 3013496867
- 1250045
- 1320894
- 3031092085
- 3042205143
- 3017390965
- 9681544
- 2435947
- 3010018659
Source Documents#
Other 510(k) Records For Product Code MGQ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K171879 | HylaGuard Moisturizing Cream | Founders Science Group, LLC | 2017-10-16 |
| K083024 | HYLATOPIC EMOLLIENT FOAM | Collegium Pharmaceutical Incorporated | 2009-03-27 |
| K041342 | IMPRUV A.I. CREAM WOUND AND SKIN EMULSION | Stiefel Laboratories, Inc. | 2005-07-19 |
| K041268 | SILVERSITE OR CALGITROL | Adri | 2004-09-20 |
| K040019 | SILVERSEAL | Noble Fiber Technologies | 2004-07-23 |
| K040517 | TENDERWET ACTIVE | Medline Industries, Inc. | 2004-03-25 |
| K022587 | MEDTRADE PRODUCT'S ANTISEPTIC BARRIER HYDROGEL DRESSINGS | Medtrade Products , Ltd. | 2003-08-22 |
| K024367 | SINCLAIR WOUND AND SKIN EMULSION | Sinclair Pharmaceuticals, Ltd. | 2003-07-28 |
| K024054 | XYLOS XCELL ANTIMICROBIAL DRESSING | Xylos Corporation | 2003-03-07 |
| K022584 | CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING | Cardiotech Intl. | 2002-12-30 |
| K022995 | COLLATEK HYDROGEL | Biocore Medical Technologies, Inc. | 2002-12-02 |
| K013525 | CONTREET-H ANTIMICROBIAL HYDROCOLLOID DRESSING, MODELS 9610 (4 X 4 (10 CM X 10CM), 9613 (6X6 (15CM X 15CM) | Coloplast Corp. | 2002-10-04 |
| K020325 | L.A.M. IPM WOUND GEL | L.A.M. Pharmaceutical, Corp. | 2002-04-15 |
| K011994 | ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101 | Acrymed, Inc. | 2001-11-08 |
| K010583 | AMBU GEL, HYDROGEL BURN DRESSING | Ambu, Inc. | 2001-05-25 |
Legacy Summary#
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FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases