Atlas FDA

INTERSORB LAPAROTOMY SPONGE

FDA 510(k) clearance K761037 · decided 1976-12-29

Clearance details

K-number
K761037
Device name
INTERSORB LAPAROTOMY SPONGE
Applicant
Chesebrough-Pond'S U.S.A. Co.
Decision
Substantially Equivalent
Date received
1976-11-15
Decision date
1976-12-29
Days to decision
44 days
Clearance type
Traditional
Product code
EFQ
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
NON-ABSORBABLE GAUZE FOR EXTERNAL USE, STERILE AND NON STERILE (K991757)Furlong Industries1999-08-12
SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S (K991215)Symtex Healthcare Corp.1999-06-11
VITOP DRESSING (K990974)Wonder & Bioenergy Hi-Tech America, Inc.1999-06-09
GAUZE SPONGES: LAPAROTOMY SPONGE, X-RAY DETECTABLE (K990584)Broadline Medical Industries1999-04-23
CROSSTEX NON-WOVEN SPONGES (K984187)Crosstex Intl.1999-02-18
GAUZE, SPONGES, CAT # 11-003 (K983016)Vitalcare Group, Inc.1999-02-12
DYNAREX TRACHEOSTOMY SPONGE (K983348)Dynarex Corp.1998-12-11
STARRYSHINE GAUZE SPONGE (K983450)T.C. Dental Products, Inc.1998-11-12
JOAN II (K982648)Celanese Acetate Co.1998-09-30
DUMEX PAK-ITS WOVEN RIBBON PACKING (K980791)Dumex Medical Surgical Products, Ltd.1998-04-29
HYDROFERA FEMORAL WICK (K974316)Hydrofera, LLC1998-02-13
BALDUR NON-STERILE COTTON SPONGES (K974347)Baldur Systems Corp.1998-02-10

Recalls involving this device

No recalls on record reference this clearance.