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

BOUFFANT CAP

K Number: K882283 · Decision Jun 23, 1988
Classifications
1
FEI Numbers
291
Registration Numbers
291
Same Product Code
31
Applicant Total
11
Review Days
23

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Basic Information

Device Name
BOUFFANT CAP
K Number
K882283
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
FYF
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FYF Cap, 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
K882281 GOWN, ISOLATION, SURGICAL (FYC)
K882284 SURGEONS CAP
K882282 SUIT, SURGICAL
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. →