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

BERKELEY V-10 VACUUM CURETTAGE SYSTEM

K Number: K030935 · Decision Jun 23, 2003
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
23
Applicant Total
16
Review Days
90

Basic Information

Device Name
BERKELEY V-10 VACUUM CURETTAGE SYSTEM
K Number
K030935
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5070
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ACMI CORPORATION
Date Received
March 25, 2003
Decision Date
June 23, 2003
Product Code
HHI
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
HHI System, Abortion, Vacuum

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