Atlas FDA

SURGICAL GOWN

FDA 510(k) clearance K912790 · decided 1991-09-19

Clearance details

K-number
K912790
Device name
SURGICAL GOWN
Applicant
Unicor Federal Dept. of Justice
Decision
Substantially Equivalent
Date received
1991-06-25
Decision date
1991-09-19
Days to decision
86 days
Clearance type
Traditional
Product code
FYE
Device class
1
Regulation number
878.4040
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Alderson, WV, 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
BARRIER* EXTRA PROTECTION PLUS SURGICAL GOWN (K932731)Johnson & Johnson Medical, Inc.1994-04-11
PROTEKT GLOVES (K910920)Intermedics Orthopedics1991-05-15
LIFELINER SURGICAL GLOVE (K910941)Depuy-Raynham1991-05-09
STERILE SURGICAL GOWN (K895667)Clinitech, Inc.1989-10-13
VARIOUS DISPOSABLE SURGICAL GARMENTS (K895235)Protect Corp. of Indiana, Inc.1989-09-19
CLOTHINGUARD (K894760)Barrier Concepts, Inc.1989-08-18

Recalls involving this device

No recalls on record reference this clearance.