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

AMCATH SUCTION-IRRIGATION TUBE

K Number: K900988 · Decision May 7, 1990
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
17
Review Days
66

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Basic Information

Device Name
AMCATH SUCTION-IRRIGATION TUBE
K Number
K900988
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Intl. Medical, Inc.
Date Received
March 2, 1990
Decision Date
May 7, 1990
Product Code
HET
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
HET Laparoscope, Gynecologic (And Accessories)

Similar 510(k) Clearances

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Other Clearances by Intl. Medical, Inc.

K Number Device Name
K970507 PEAK FLOW METER
K943078 HOT BIOPSY FORCEPS
K940370 AMERICAN CATHETER E.R.C.P. CANNULA
K940335 AMERICAN CATHETER POLY-SNARE
K942068 AMERICAN CATHETER SPHINCTEROTOME
K930406 DURHAM; MIN BORE LUER LOCK EXTENSION SET
K930410 DURHAM; LUER LOCK EXTENSION SET
K923200 AMCATH DISPOSABLE CYTOLOGY BRUSH
K915142 AMCATH DISPOSABLE BIOPSY FORCEPS
K912927 AMCATH DISPOSABLE TROCAR AND TROCAR SLEEVE
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