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

INSUFFLATOR

K Number: K812200 · Decision Sep 29, 1981
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
9
Review Days
56

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Basic Information

Device Name
INSUFFLATOR
K Number
K812200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Reznik Instruments
Date Received
August 4, 1981
Decision Date
September 29, 1981
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 Reznik Instruments

K Number Device Name
K812205 FORCEP
K812201 PHOTOGRAPHIC EQUIPMENT
K812203 ELECTROSURGICAL UNIT
K812206 LAPAROSCOPE
K812199 TROCAR & TROCAR SLEEVES
K812204 UTERINE MANIPULATORS
K812202 FIBER OPTIC LIGHT SOURCE
K812198 ACCESSORIES(PROBES, SUCTION TUBES, ETC.)