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FDA 510(k)

INMAN POOLE TIP SUCTION PROBE W/TUBING KIT

K-Number: K933170 · 1993-09-16

ApplicantInman Medical Corp.
Decision Date1993-09-16
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INMAN POOLE TIP SUCTION PROBE W/TUBING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Inman Medical Corp.. It received FDA 510(k) clearance on 1993-09-16 under 510(k) number K933170. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INMAN POOLE TIP SUCTION PROBE W/TUBING KIT?

INMAN POOLE TIP SUCTION PROBE W/TUBING KIT is a medical device that received FDA 510(k) clearance on 1993-09-16. The listed applicant is Inman Medical Corp.. The 510(k) number is K933170.

When did INMAN POOLE TIP SUCTION PROBE W/TUBING KIT receive FDA 510(k) clearance?

INMAN POOLE TIP SUCTION PROBE W/TUBING KIT received FDA 510(k) clearance on 1993-09-16, under 510(k) number K933170.

Who is the listed applicant for INMAN POOLE TIP SUCTION PROBE W/TUBING KIT?

The FDA 510(k) record lists Inman Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INMAN POOLE TIP SUCTION PROBE W/TUBING KIT?

The FDA product code for INMAN POOLE TIP SUCTION PROBE W/TUBING KIT is GCY.

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Other records listing Inman Medical Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K933171INMAN IRRIGATION TAPERED PROBEK933169INMAN ENDOSCOPIC BLUNT DISSECTORK933094INSUFFLATOR TUBING KIT W/FILTERK933382IMC CABLE/WIRE COVERK933774IMC SALINE WET DRESSINGK933305IMC 5.0MM IRRIGATION/ASPIRATION PROBE

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Related Devices (Code: GCY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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