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

INTESTINAL CLAMP

K Number: K890372 · Decision Feb 3, 1989
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
13
Applicant Total
63
Review Days
11

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Basic Information

Device Name
INTESTINAL CLAMP
K Number
K890372
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Kinetic Medical Products
Date Received
January 23, 1989
Decision Date
February 3, 1989
Product Code
HXD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
HXD Clamp

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