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

CLAMP-N-CUT

K Number: K860445 · Decision Apr 4, 1986
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
35
Applicant Total
3
Review Days
59

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Basic Information

Device Name
CLAMP-N-CUT
K Number
K860445
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Mmi, Inc.
Date Received
February 4, 1986
Decision Date
April 4, 1986
Product Code
HFW
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
HFW Clamp, Umbilical

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Other Clearances by Mmi, Inc.

K Number Device Name
K905026 DUAL FLEX NON-LATEX
K842130 G.I. CLEANSING KIT