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FDA 510(k)

ELECTROSURGICAL CAUTERY PROBES

K-Number: K981188 · 1998-05-20

ApplicantMicroline Pentax, Inc.
Decision Date1998-05-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL CAUTERY PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Microline Pentax, Inc.. It received FDA 510(k) clearance on 1998-05-20 under 510(k) number K981188. 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 ELECTROSURGICAL CAUTERY PROBES?

ELECTROSURGICAL CAUTERY PROBES is a medical device that received FDA 510(k) clearance on 1998-05-20. The listed applicant is Microline Pentax, Inc.. The 510(k) number is K981188.

When did ELECTROSURGICAL CAUTERY PROBES receive FDA 510(k) clearance?

ELECTROSURGICAL CAUTERY PROBES received FDA 510(k) clearance on 1998-05-20, under 510(k) number K981188.

Who is the listed applicant for ELECTROSURGICAL CAUTERY PROBES?

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

What is the FDA product code for ELECTROSURGICAL CAUTERY PROBES?

The FDA product code for ELECTROSURGICAL CAUTERY PROBES is GEI.

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Official Source

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

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