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

NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC

K Number: K863201 · Decision Aug 29, 1986
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
95
Applicant Total
33
Review Days
10

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Basic Information

Device Name
NEW USE FOR ACUVAC SUCTION RESERVOIR 400CC
K Number
K863201
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Allergan, Inc.
Date Received
August 19, 1986
Decision Date
August 29, 1986
Product Code
GCY
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
GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

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K051852 SINGLE AMPLIFIER FOR BOTOX
K014202 COMPLETE BRAND MULTI-PURPOSE SOLUTION
K013479 COMPLETE BRAND MULTI-PURPOSE SOLUTION
K003252 COMPLETE BRAND MULTI-PURPOSE SOLUTION
K003638 MOJAVE CATARACT EXTRACTION SYSTEM
K003109 COMPLETE BRAND LUBRICATING AND REWETTING DROPS
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