510(k) K820108
- Device
- TOPPER SPONGES
- Applicant
- STAN-PAK ENT.
- 510(k) number
- K820108
- Product code
- NAB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-02-12
- Date received
- 1982-01-15
- 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#
- 1422634
- 3007344957
- 3010621964
- 3031167704
- 3022954003
- 3008386507
- 3015895045
- 3034669683
- 3004513970
- 3038162648
- 3002637602
- 1053541
- 1423662
- 3010864832
- 3008264111
- 3030896267
- 3019315696
- 3008851420
- 3005951296
- 2083545
- 3008485841
- 3017297225
- 3009114792
- 3017107376
- 3012050423
- 3016452400
- 3004125670
- 3012818008
- 3010374972
- 3007480628
- 3003403221
- 3011849720
- 3039394934
- 3007299770
- 3004753358
- 3007187674
- 3007966889
- 3005558160
- 3009605026
- 3042367543
- 3035786158
- 1054241
- 3042283853
- 1052728
- 3015437221
- 3038274448
- 3010583458
- 3039388855
- 3011767135
- 3003915875
- 3008255748
- 3025384290
- 3005112833
- 3009167225
- 3033011342
- 9616518
- 3003887292
- 3042032212
- 9616872
- 3008494300
- 3031184338
- 3011238790
- 3012660022
- 3016195240
- 3045857302
- 3011434305
- 3009756153
- 3010967704
- 3010339057
- 3012421607
- 3007305426
- 3014146451
- 3015378469
- 1250045
- 3013632692
- 9612354
- 3017367014
- 3017095924
- 3018228713
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 |
| K923116 | COMBINE II WETPROOF PAD | Hermitage Hospital Products, Inc. | 1992-10-06 |
| 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 |
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