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

PACER DISPOSABLE YANKAUER SUCTION INSTRUMENT

K Number: K921095 · Decision Apr 29, 1992
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
1
Review Days
54

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Basic Information

Device Name
PACER DISPOSABLE YANKAUER SUCTION INSTRUMENT
K Number
K921095
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pacer Tool & Plastics, Inc.
Date Received
March 6, 1992
Decision Date
April 29, 1992
Product Code
GBX
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
GBX Catheter, Irrigation

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