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FDA 510(k)

DISP. YANKAVER SURG. SUCTION INSTRUMENT

K-Number: K830123 · 1983-06-08

ApplicantNarco Scientific
Decision Date1983-06-08
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISP. YANKAVER SURG. SUCTION INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K830123. 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 DISP. YANKAVER SURG. SUCTION INSTRUMENT?

DISP. YANKAVER SURG. SUCTION INSTRUMENT is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Narco Scientific. The 510(k) number is K830123.

When did DISP. YANKAVER SURG. SUCTION INSTRUMENT receive FDA 510(k) clearance?

DISP. YANKAVER SURG. SUCTION INSTRUMENT received FDA 510(k) clearance on 1983-06-08, under 510(k) number K830123.

Who is the listed applicant for DISP. YANKAVER SURG. SUCTION INSTRUMENT?

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

What is the FDA product code for DISP. YANKAVER SURG. SUCTION INSTRUMENT?

The FDA product code for DISP. YANKAVER SURG. SUCTION INSTRUMENT is GCY.

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Other records listing Narco Scientific as applicant

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Related Devices (Code: GCY)

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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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