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

CURETTE, UTERINE, VACUUM ASPIRATING

K Number: K770674 · Decision Apr 26, 1977
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
41
Applicant Total
56
Review Days
15

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Basic Information

Device Name
CURETTE, UTERINE, VACUUM ASPIRATING
K Number
K770674
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1175
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
American Hospital Supply Corp.
Date Received
April 11, 1977
Decision Date
April 26, 1977
Product Code
HHK
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
HHK Curette, Suction, Endometrial (And Accessories)

Similar 510(k) Clearances

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Other Clearances by American Hospital Supply Corp.

K Number Device Name
K854739 AMERICAN STERILE SURGICAL ABSORBENT TOWEL
K854759 AMERICAN STERILE MAYO STAND TRAY
K832826 AAP DOSIMETRY RELEASE OR BASIN SETS
K830546 DOSIMETRIC RELEASE
K822990 CONVERTORS PRIMARY WOUND DRESSING II
K830343 CONTAINER W/PRIMING SOLUTION
K830301 STRATUS FLUOROMETRIC ENZYME IMMUN0-
K822755 LATEX PENROSE TUBING
K823418 HEYER-SCHUTE UNIVERSAL URETERAL STENT
K822966 CONVERTORS DISPOSABLE DRESSING SPONGE
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