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

INSUFFLATION NEEDLE, MODEL R65-933

K Number: K000027 · Decision Apr 3, 2000
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
23
Review Days
89

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Basic Information

Device Name
INSUFFLATION NEEDLE, MODEL R65-933
K Number
K000027
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
A & A Medical, Inc.
Date Received
January 5, 2000
Decision Date
April 3, 2000
Product Code
HIF
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
HIF Insufflator, Laparoscopic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HIF), ordered by most recent decision date.

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Other Clearances by A & A Medical, Inc.

K Number Device Name
K013437 SF SH CATHETER, MODEL R65-945
K013491 HSG CATHETER SET, 5F MODEL RGS0947, HSG CATHETER SET, 7F, MODEL R65-948
K003949 TACKER, MODEL R65-933
K011512 MMODIFICATION TO LAMINARIA
K010510 BALLOON CANNULA, SHORT, MODEL R65-985; BALLOON CANNULA, LONG, MODEL R65-985-1
K010789 CANNULA, SURGICAL GENERAL & PLASTIC SURGERY, MODELR65-995, R65-995-1, R65-995-2, R65-997, R65-997-1
K010056 UTERINE MANIPULATOR INJECTOR CANNULA, STERILE, MODEL R 57-450
K994256 SUCTION IRRIGATION TRUMPET VALVE SET, MODEL Q65-823
K974038 THE ASPIRATOR, 6FT SILICONE TUBING, METAL TUBING ADAPTER, GLASS RESERVOIR, NEOPRENE STOPPER, ANGLED TUBE MOUNTS, FOOT
K974138 ROCKET ELECTRODE
Search all 23 clearances from A & A Medical, Inc. →