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

MICROINFERTILITY SCISSORS, TITANIUM

K Number: K844822 · Decision Jan 16, 1985
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
57
Applicant Total
3
Review Days
37

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Basic Information

Device Name
MICROINFERTILITY SCISSORS, TITANIUM
K Number
K844822
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Precision Surgical Instrument, Inc.
Date Received
December 10, 1984
Decision Date
January 16, 1985
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

Similar 510(k) Clearances

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

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Other Clearances by Precision Surgical Instrument, Inc.

K Number Device Name
K844821 MICROINFERTILITY NEEDLE HOLDER, TITANIUM
K844823 MICROINFERTILITY FORCEPS, TITANIUM