10.0MM Suction/Irrigation Probe & Tubing Kit

FDA 510(k) K932762 · Inman Medical Corp.

Substantially Equivalent

510(k) numberK932762

Submission

Device name
10.0MM Suction/Irrigation Probe & Tubing Kit
Applicant
Inman Medical Corp.
Fort Worth, TX, US
Received
June 8, 1993
Decision date
August 31, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GCS – Endoscope, Battery-Powered And Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

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K933201Aesculap Trocar Instrument SetGCS · Traditional Aesculap, Inc.09/13/1993SE
K933371Imc Endoscopic Instrument HolderGCS · Traditional Inman Medical Corp.08/06/1993SE
K924134Leisegang Laparoscopic Irrigation System/AccessGCS · Traditional Leisegang Medical, Inc.07/02/1993SE
K931340Grasp Forceps/Scissors/Needle Holder/DissectorGCS · Traditional Baxter Healthcare Corp07/01/1993SE
K925276M.I.S. Trocar-CannulaGCS · Traditional M.I.S. Technology, Inc.05/24/1993SE
K921006Laparoscopic Retractor SystemGCS · Traditional Laparomed Corp.07/28/1992SE

More from Laparomed Corp.

510(k)DeviceDecision
K933171Inman Irrigation Tapered ProbeKYZ · Traditional 04/29/1994SE
K933169Inman Endoscopic Blunt DissectorGCJ · Traditional 04/19/1994SE
K933094Insufflator Tubing Kit W/FilterHIF · Traditional 04/18/1994SE
K933382Imc Cable/Wire CoverKKX · Traditional 01/27/1994SE
K933774Imc Saline Wet DressingFRO · Traditional 11/08/1993SN
K933306Imc 5.0MM Irrigation/Aspiration Probe W/HolesGCY · Traditional 10/05/1993SE
K933305Imc 5.0MM Irrigation/Aspiration ProbeGCY · Traditional 10/05/1993SE
K933170Inman Poole Tip Suction Probe W/Tubing KitGCY · Traditional 09/16/1993SE
K933371Imc Endoscopic Instrument HolderGCS · Traditional 08/06/1993SE
K921291Inman Medical Packing StripFER · Traditional 01/21/1993SE

Questions and answers

When was 10.0MM Suction/Irrigation Probe & Tubing Kit cleared by the FDA?

10.0MM Suction/Irrigation Probe & Tubing Kit (K932762) received a 510(k) decision of Substantially Equivalent on August 31, 1993, 84 days after the submission was received.

What is the product code of K932762?

The FDA product code is GCS – Endoscope, Battery-Powered And Accessories, a Class II (moderate risk) device regulated under 21 CFR 876.1500.