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

SURGICAL PROBE

K Number: K890227 · Decision Jan 27, 1989
Classifications
1
FEI Numbers
373
Registration Numbers
373
Same Product Code
14
Applicant Total
63
Review Days
9

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Basic Information

Device Name
SURGICAL PROBE
K Number
K890227
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Kinetic Medical Products
Date Received
January 18, 1989
Decision Date
January 27, 1989
Product Code
HXB
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HXB Probe

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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
K890216 MICROSURGICAL KERATOME
K890378 UTERINE DRESSING FORCEPS
K890379 UTERINE TENTACULUM
K890389 UMBILICAL SCISSORS
Search all 63 clearances from Kinetic Medical Products →