ClearanceBrief
Company ยท US

Reznik Instruments

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1981. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEIElectrosurgical, Cutting & Coagulation & Accessories2
HETLaparoscope, Gynecologic (And Accessories)2
FEMAccessories, Photographic, For Endoscope (Exclude Light Sources)1
GENForceps, General & Plastic Surgery1
HIFInsufflator, Laparoscopic1
HIHHysteroscope (And Accessories)1
KOHInstrument, Manual, General Obstetric-Gynecologic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 26, 1981K812205FORCEP
Reznik Instruments
GEN
Oct 19, 1981K812201PHOTOGRAPHIC EQUIPMENT
Reznik Instruments
FEM
Oct 13, 1981K812206LAPAROSCOPE
Reznik Instruments
HET
Oct 13, 1981K812204UTERINE MANIPULATORS
Reznik Instruments
KOH
Oct 13, 1981K812203ELECTROSURGICAL UNIT
Reznik Instruments
GEI
Oct 13, 1981K812199TROCAR & TROCAR SLEEVES
Reznik Instruments
HET
Sep 29, 1981K812202FIBER OPTIC LIGHT SOURCE
Reznik Instruments
HIH
Sep 29, 1981K812200INSUFFLATOR
Reznik Instruments
HIF
Sep 11, 1981K812198ACCESSORIES(PROBES, SUCTION TUBES, ETC.)
Reznik Instruments
GEI

Latest recalls

DateFirm and productCodeLinked 510(k)
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