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FDA 510(k)

VENT TUBE FORCEPS

K-Number: K831589 · 1983-06-16

ApplicantTreace Medical, Inc.
Decision Date1983-06-16
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VENT TUBE FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Treace Medical, Inc.. It received FDA 510(k) clearance on 1983-06-16 under 510(k) number K831589. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENT TUBE FORCEPS?

VENT TUBE FORCEPS is a medical device that received FDA 510(k) clearance on 1983-06-16. The listed applicant is Treace Medical, Inc.. The 510(k) number is K831589.

When did VENT TUBE FORCEPS receive FDA 510(k) clearance?

VENT TUBE FORCEPS received FDA 510(k) clearance on 1983-06-16, under 510(k) number K831589.

Who is the listed applicant for VENT TUBE FORCEPS?

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

What is the FDA product code for VENT TUBE FORCEPS?

The FDA product code for VENT TUBE FORCEPS is EQH.

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Other records listing Treace Medical, Inc. 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.

K883727BUCKET PROSTHESIS PORPK882349MALLET, SURGICALK874779BIPOLATOR 50K873154TREACE MAGNUM OTO-TOOL SYSTEMK872000EYE GARDK870765CANNULATED INSTRUMENT CLEANERS

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Related Devices (Code: EQH)

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.

K945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTWells Johnson Co.K954184JED-LIGHT FIBEROPTIC LIGHT SOURCEJedmed Instrument Co.K951829COLD LIGHT SOURCE LOS 150Laser-Optik-Systeme GmbH & Co. KGK932771BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCEXomed-Treace, Inc.K941661GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHTGm Engineering, Inc.K941662GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHTGm Engineering, 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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