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

BERACLAMP, MODEL BC-1

K Number: K990045 · Decision May 24, 1999
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
57
Applicant Total
1
Review Days
138

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Basic Information

Device Name
BERACLAMP, MODEL BC-1
K Number
K990045
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Poamax LLC
Date Received
January 6, 1999
Decision Date
May 24, 1999
Product Code
KNA
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNA Instrument, Manual, Specialized Obstetric-Gynecologic

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