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FDA 510(k)

SUCTION CAUTERY PROBE

K-Number: K955352 · 1996-04-05

ApplicantMectra Labs, Inc.
Decision Date1996-04-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUCTION CAUTERY PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Mectra Labs, Inc.. It received FDA 510(k) clearance on 1996-04-05 under 510(k) number K955352. 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 SUCTION CAUTERY PROBE?

SUCTION CAUTERY PROBE is a medical device that received FDA 510(k) clearance on 1996-04-05. The listed applicant is Mectra Labs, Inc.. The 510(k) number is K955352.

When did SUCTION CAUTERY PROBE receive FDA 510(k) clearance?

SUCTION CAUTERY PROBE received FDA 510(k) clearance on 1996-04-05, under 510(k) number K955352.

Who is the listed applicant for SUCTION CAUTERY PROBE?

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

What is the FDA product code for SUCTION CAUTERY PROBE?

The FDA product code for SUCTION CAUTERY PROBE is GEI.

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Other records listing Mectra Labs, Inc. as applicant

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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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