510(k) K823879
- Device
- COVER-ROLL STRETCH
- Applicant
- BEIERSDORF, INC.
- 510(k) number
- K823879
- Product code
- NAB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1983-03-09
- Date received
- 1982-12-27
- Regulation
- 878.4014
- Classification name
- Gauze / Sponge,nonresorbable For External Use
- Medical specialty
- General & Plastic Surgery
- Review panel
- General & Plastic Surgery
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3017248120
- 3023809973
- 3015379055
- 3015214015
- 3032172199
- 3019543072
- 2431166
- 3006400320
- 3010952189
- 3012660022
- 1250045
- 2029275
- 3005360866
- 3026263452
- 3006787036
- 3007615588
- 3016807211
- 3017461134
- 3009308092
- 3005621808
- 3038162648
- 3007305426
- 3003348807
- 3004547763
- 3004176951
- 3012940386
- 3006973666
- 3013466775
- 3031982537
- 3031288561
- 3015219076
- 3017059795
- 3018228713
- 3008773774
- 3005951296
- 2083545
- 3001650535
- 3003887292
- 3005735974
- 3006538822
- 3008392711
- 3004519921
- 3010583458
- 3010598169
- 3006065092
- 3007007790
- 3031590640
- 3003674698
- 3005524530
- 1061124
- 9611462
- 3011529314
- 3009148458
- 3008386507
- 3021349683
- 3003528228
- 2530957
- 1053541
- 3006847937
- 3010515547
- 2648727
- 3007479164
- 9616874
- 9611459
- 1055236
- 1025972
- 3009307523
- 3012314549
- 3015738552
- 3030394731
- 3008676146
- 3012268821
- 1045254
- 3043106338
- 9680271
- 3013557562
- 3045855232
- 2437780
- 3010131137
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code NAB #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K946015 | IVALON EXTERNAL SPONGE | Ivalon | 1995-02-27 |
| K940755 | ISOLYER (4X4, 8PLY) | Isolyer Co. | 1994-05-02 |
| K931610 | OMNISORB II, NONWOVEN SPONGE, STERILE AND NON | Omni Mfg., Inc. | 1993-06-24 |
| K925590 | MULTI-TRAUMA DRESSING | Gam Industries, Inc. | 1993-04-08 |
| K926072 | K-BAND AND K-CREPE | Parema , Ltd. | 1993-03-19 |
| K915591 | STERILE GAUZE PADS | Eagle Medical, Inc. | 1993-01-27 |
| K924650 | GAUZE SPONGES | Dav-Mar Medical Products, Inc. | 1993-01-11 |
| K923602 | ABSORBENT PAD -- MODIFICATION | Winfield Laboratories, Inc. | 1992-12-07 |
| K923115 | CLINISORB | Hermitage Hospital Products, Inc. | 1992-11-23 |
| K923378 | USP TYPE VII GAUZE SPONGES | E.W.A., Ltd. | 1992-10-06 |
| K923846 | BURN DRESSING | Medical Action Industries, Inc. | 1992-09-11 |
| K915821 | MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES | Kerma Medical Products, Inc. | 1992-05-29 |
| K920282 | PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE | Trinity Laboratories, Inc. | 1992-05-29 |
| K921227 | TENCEL TOPICAL WOUND DRESSING/SURGICAL SPONGE | Courtaulds Fibers, Inc. | 1992-05-29 |
| K920269 | EZ GAUZE SPONGE | Cal West Trading Co. | 1992-04-22 |
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