FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SUIT, SURGICAL

K Number: K882282 · Decision Jun 23, 1988
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
5
Applicant Total
11
Review Days
23

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Basic Information

Device Name
SUIT, SURGICAL
K Number
K882282
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
A Plus International, Inc.
Date Received
May 31, 1988
Decision Date
June 23, 1988
Product Code
FXO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FXO Suit, Surgical

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Other Clearances by A Plus International, Inc.

K Number Device Name
K213001 Procedure Mask, Surgical Mask
K102861 SURGIPLUS SMS SURGICAL DRAPE (STERILE/NON-STERILE), SURGIPLUS SPP WITH PE LAMINATED SURGICAL DRAPE (STERILE/NON-STERILE)
K093169 SURGIPLUS STANDARD SURGICAL GOWN (STERILE) ( NON STERILE), REINFORCED SURGICAL GOWN (STERILE) (NON STERILE)
K031353 SOLUTION FACE MASKS
K882283 BOUFFANT CAP
K882281 GOWN, ISOLATION, SURGICAL (FYC)
K882284 SURGEONS CAP
K882280 COVER, SHOE OPERATING ROOM
K881396 OPERATING ROOM TOWELS -STERILE & NON-STERILE
K881395 GAUZE AND LAP SPONGES -STERILE & NON-STERILE
Search all 11 clearances from A Plus International, Inc. →