FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MICROSURGICAL KERATOME

K Number: K890216 · Decision Feb 16, 1989
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
12
Applicant Total
63
Review Days
29

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Basic Information

Device Name
MICROSURGICAL KERATOME
K Number
K890216
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.4525
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Kinetic Medical Products
Date Received
January 18, 1989
Decision Date
February 16, 1989
Product Code
GZX
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GZX Instrument, Microsurgical

Similar 510(k) Clearances

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Other Clearances by Kinetic Medical Products

K Number Device Name
K890385 MIDWIFERY/OBSTETRICAL FORCEPS
K890387 MALLEABLE PLACENTA CURETTE
K890380 CERVICAL BIOPSY FORCEPS
K890382 COMPRESSION FORCEPS
K890376 VAGINAL SPECULUM
K890383 HYSTERECTOMY FORCEPS
K890378 UTERINE DRESSING FORCEPS
K890379 UTERINE TENTACULUM
K890389 UMBILICAL SCISSORS
K890377 FIXED-SIZE UTERINE DILATOR
Search all 63 clearances from Kinetic Medical Products →