Atlas FDA

STERILIZATION PROCESS/X-RAY DETECT. SPG

FDA 510(k) clearance K792630 · decided 1980-01-11

Clearance details

K-number
K792630
Device name
STERILIZATION PROCESS/X-RAY DETECT. SPG
Applicant
Procter & Gamble Mfg. Co.
Decision
Substantially Equivalent
Date received
1979-12-19
Decision date
1980-01-11
Days to decision
23 days
Clearance type
Traditional
Product code
GDY
Device class
1
Regulation number
878.4450
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
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
ULTRACELL SUCTION SPONGE (K972634)Ultracell Medical Technologies, Inc.1997-12-17
CPR LAP SPONGES (K960236)Custom Pack Reliability1996-03-28
STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE (K955599)Stryker Corp.1996-02-22
PROTEC X-RAY DETECTABLE GAUZE SPONGE (K955322)Derivados DE Gasa, S.A. DE C.V.1995-12-19
KENSORB (K953830)Kentron Health Care, Inc.1995-10-03
ROSEBUD DISSECTOR (K953060)Medical Perspectives Corp.1995-09-14
CHERRY PIT DISSECTOR (K953087)Medical Perspectives Corp.1995-09-14
CYLINDRICAL SPONGE (K953057)Medical Perspectives Corp.1995-09-14
ROUND STICK SPONGES, FLAT STICK SPONGES (K953058)Medical Perspectives Corp.1995-09-14
TRIANGULAR SPONGES (K953088)Medical Perspectives Corp.1995-09-14
KITTNER DISSECTOR (K953059)Medical Perspectives Corp.1995-09-14
CHERRY DISSECTOR (K953062)Medical Perspectives Corp.1995-09-14

Recalls involving this device

No recalls on record reference this clearance.