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

MITYVAC DISPOS-A-PLATE DISPOSABLE LEG PLATE

K Number: K925572 · Decision Oct 8, 1993
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
213
Applicant Total
8
Review Days
339

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Basic Information

Device Name
MITYVAC DISPOS-A-PLATE DISPOSABLE LEG PLATE
K Number
K925572
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2740
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Neward Enterprises, Inc.
Date Received
November 3, 1992
Decision Date
October 8, 1993
Product Code
HGM
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
HGM System, Monitoring, Perinatal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HGM), ordered by most recent decision date.

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Other Clearances by Neward Enterprises, Inc.

K Number Device Name
K960549 MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE
K943938 MITYVAC SUPER M STYLE VACUM EXTRACTOR, DISPOSABLE
K934011 MITYVAC(R) OBSTETRIC VAC DELIV KIT W/UNIV VAC RELEASE
K913324 MITYVAC(R) SAFTISOFT OBSTETRICAL VACUUM DELIV KIT
K910815 CR SPIRAL ELECTRODE
K890307 MITYVAC M STYLE VACUUM EXTRACTOR, DISPOSABLE
K840403 VENA * BRIDGE