510(k) K791726
- Device
- HYDROGEL-PREP
- Applicant
- SPENCO MEDICAL CORP.
- 510(k) number
- K791726
- Product code
- NAB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-11-20
- Date received
- 1979-09-04
- 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#
- 1051614
- 3010363542
- 3003965134
- 3009526336
- 3010199022
- 2029234
- 3003062321
- 3038274448
- 1221254
- 3030067857
- 3004361903
- 3043648115
- 3006425876
- 3010583458
- 3024891479
- 3003528228
- 1000115322
- 3007480628
- 3009931872
- 3043226252
- 3011529314
- 3031481777
- 3023339277
- 3042953785
- 3008773774
- 3049077135
- 3031789039
- 3015989868
- 3016171961
- 3011611571
- 3016457665
- 3011050570
- 3013524663
- 3013547614
- 3010187826
- 1724809
- 3015337116
- 3016837630
- 1222313
- 3014108257
- 3016450032
- 3009563903
- 9613778
- 3033011342
- 3039282838
- 3010957766
- 3009155880
- 3004617181
- 3023191945
- 3007479164
- 3008851420
- 3012677665
- 3009167225
- 3015437221
- 3008496560
- 3008264242
- 3003807757
- 3007865243
- 3011193403
- 3003835287
- 3031590640
- 1219313
- 3009148458
- 3026331889
- 3011707926
- 2086484
- 3042283853
- 3043051314
- 3031184338
- 3012311599
- 3006891803
- 3016816754
- 1824619
- 3044995512
- 1043214
- 3012711490
- 3015414875
- 3024088964
- 3035382642
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