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

SUCTION REGULATOR 7700 SERIES

K Number: K850200 · Decision Mar 4, 1985
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
20
Applicant Total
37
Review Days
45

Basic Information

Device Name
SUCTION REGULATOR 7700 SERIES
K Number
K850200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
BOEHRINGER LABORATORIES
Date Received
January 18, 1985
Decision Date
March 4, 1985
Product Code
KDP
Advisory Committee
General Hospital
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
KDP Regulator, Vacuum

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