FDA 510(k)

GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435

K-Number: K994075 · 1999-12-27

ApplicantGeiger Medical Technologies, Inc.

Decision Date1999-12-27

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435 is the device name listed in this FDA 510(k) record. The listed applicant is Geiger Medical Technologies, Inc.. It received FDA 510(k) clearance on 1999-12-27 under 510(k) number K994075. 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 GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435?

GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435 is a medical device that received FDA 510(k) clearance on 1999-12-27. The listed applicant is Geiger Medical Technologies, Inc.. The 510(k) number is K994075.

When did GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435 receive FDA 510(k) clearance?

GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435 received FDA 510(k) clearance on 1999-12-27, under 510(k) number K994075.

Who is the listed applicant for GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435?

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

What is the FDA product code for GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435?

The FDA product code for GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435 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.