FDA 510(k)

GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405

K-Number: K992149 · 1999-08-19

ApplicantGeiger Medical Technologies, Inc.

Decision Date1999-08-19

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405 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 1999-08-19 under 510(k) number K992149. 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 ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405?

GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405 is a medical device that received FDA 510(k) clearance on 1999-08-19. The listed applicant is Geiger Medical Technologies, Inc.. The 510(k) number is K992149.

When did GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405 receive FDA 510(k) clearance?

GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405 received FDA 510(k) clearance on 1999-08-19, under 510(k) number K992149.

Who is the listed applicant for GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405?

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 ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405?

The FDA product code for GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405 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.