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FDA 510(k)

SMOKE EVACUATION ATTACHMENT 130XXX TBD

K-Number: K982309 · 1998-08-05

ApplicantConmedcorp
Decision Date1998-08-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SMOKE EVACUATION ATTACHMENT 130XXX TBD is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1998-08-05 under 510(k) number K982309. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMOKE EVACUATION ATTACHMENT 130XXX TBD?

SMOKE EVACUATION ATTACHMENT 130XXX TBD is a medical device that received FDA 510(k) clearance on 1998-08-05. The listed applicant is Conmedcorp. The 510(k) number is K982309.

When did SMOKE EVACUATION ATTACHMENT 130XXX TBD receive FDA 510(k) clearance?

SMOKE EVACUATION ATTACHMENT 130XXX TBD received FDA 510(k) clearance on 1998-08-05, under 510(k) number K982309.

Who is the listed applicant for SMOKE EVACUATION ATTACHMENT 130XXX TBD?

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

What is the FDA product code for SMOKE EVACUATION ATTACHMENT 130XXX TBD?

The FDA product code for SMOKE EVACUATION ATTACHMENT 130XXX TBD is GEI.

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Related Devices (Code: GEI)

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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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