510(k) K760094
- Device
- SPONGE, CURITY WASHED GAUZE
- Applicant
- KENDALL RESEARCH CENTER
- 510(k) number
- K760094
- Product code
- NAB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1976-07-16
- Date received
- 1976-06-21
- 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#
- 3004513970
- 3023341288
- 3010515547
- 3010598169
- 3012034017
- 3034669683
- 3013034812
- 2245304
- 1037007
- 3032507796
- 3031600086
- 3032172199
- 1047843
- 3038718579
- 2182318
- 3011862887
- 1038758
- 3021286079
- 3003835287
- 1421873
- 3010380285
- 3013735158
- 3019804885
- 3014421917
- 3021282544
- 3039394934
- 3005735974
- 3013421458
- 3017059795
- 3027234828
- 3045855232
- 3044819802
- 2031508
- 3002637602
- 3009403363
- 3008294339
- 3016833936
- 3008264111
- 3035786158
- 3007028032
- 3007417776
- 3015379055
- 3026536498
- 3020460367
- 3011137372
- 3009167225
- 3030067857
- 1055236
- 3016452400
- 3012777736
- 3010034780
- 3007307589
- 3010864832
- 3004361903
- 3006847937
- 2135152
- 3035523371
- 3018228713
- 1319660
- 1025972
- 3010951382
- 3015214015
- 9614157
- 3003965134
- 3004569180
- 9611459
- 3015422337
- 3008663306
- 9616872
- 3013497020
- 3003528228
- 3008076203
- 3044905091
- 3013523368
- 3015139713
- 2028046
- 3012922212
- 2086484
- 3014683120
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