Inman Irrigation Tapered Probe

FDA 510(k) K933171 · Inman Medical Corp.

Substantially Equivalent

510(k) numberK933171

Submission

Device name
Inman Irrigation Tapered Probe
Applicant
Inman Medical Corp.
Fort Worth, TX, US
Received
June 29, 1993
Decision date
April 29, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KYZ – Syringe, Irrigating (Non Dental)
Device class
Class I (low risk)
Regulation
21 CFR 880.6960
Specialty
General Hospital

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More from Custom Pack Reliability

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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
K93276210.0MM Suction/Irrigation Probe & Tubing KitGCS · Traditional 08/31/1993SE
K933371Imc Endoscopic Instrument HolderGCS · Traditional 08/06/1993SE
K921291Inman Medical Packing StripFER · Traditional 01/21/1993SE

Questions and answers

When was Inman Irrigation Tapered Probe cleared by the FDA?

Inman Irrigation Tapered Probe (K933171) received a 510(k) decision of Substantially Equivalent on April 29, 1994, 304 days after the submission was received.

What is the product code of K933171?

The FDA product code is KYZ – Syringe, Irrigating (Non Dental), a Class I (low risk) device regulated under 21 CFR 880.6960.