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

CONVERTORS SURGICAL DRAPES

K Number: K993795 · Decision Jan 12, 2000
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
449
Applicant Total
63
Review Days
64

Basic Information

Device Name
CONVERTORS SURGICAL DRAPES
K Number
K993795
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ALLEGIANCE HEALTHCARE CORP.
Date Received
November 9, 1999
Decision Date
January 12, 2000
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

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Other Clearances by ALLEGIANCE HEALTHCARE CORP.

K Number Device Name
K023673 AIRLIFE DEMAND NASAL CANNULA
K023419 TRILAMINATE DRAPES/TIBURON
K024120 MODIFICATION TO TEMNO BIOPSY NEEDLES
K024292 MODIFICATION TO POSITIVE TOUCH POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN AND CHEMOTHERAPY LABELING CLAIM
K024102 DENTAL POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM
K023425 DRAPES WITH ABSORBENT REINFORCEMENT
K022765 NITRILE POWDER-FREE EXAMINATION GLOVES
K023170 NITRILE POWDER-FREE EXAMINATION GLOVES
K023167 BREATHABLE SURGICAL GOWN
K012931 GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM
Search all 63 clearances from ALLEGIANCE HEALTHCARE CORP. →