FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DRAPE SURGICAL UTILITY DRAPE STERILE

K Number: K843496 · Decision Oct 31, 1984
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
31
Review Days
55

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Basic Information

Device Name
DRAPE SURGICAL UTILITY DRAPE STERILE
K Number
K843496
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Busse Hospital Disposables, Inc.
Date Received
September 6, 1984
Decision Date
October 31, 1984
Product Code
KKX
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
KKX Drape, Surgical, Antimicrobial

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Other Clearances by Busse Hospital Disposables, Inc.

K Number Device Name
K120002 I-STYLE BONE MARROW ASPIRATION NEEDLE WITH T-HANDLE
K093909 BUSSE SURGICAL DRAPES IV
K092212 BUSSE SURGICAL DRAPES III
K082297 BUSSE SURGICAL DRAPE
K073222 MODIFICATION TO:SPECIALTY NEEDLES
K070465 BUSSE EPIDURAL CATHETER
K063018 GLASS LOSS OF RESISTANCE SYRINGE
K061394 SPECIALTY NEEDLES (SPINAL NEEDLE, PENCIL POINT SPINAL NEEDLE, EPIDURAL NEEDLE)
K061570 I-STYLE BONE MARROW ASPIRATION NEEDLE
K052843 BUSSE HOSPITAL DISPOSABLES NEEDLE STICK BLOCK/CUBE
Search all 31 clearances from Busse Hospital Disposables, Inc. →