FDA 510(k)

BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429

K-Number: K983852 · 1999-01-28

ApplicantGeiger Medical Technologies, Inc.

Decision Date1999-01-28

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429 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 1999-01-28 under 510(k) number K983852. 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 BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429?

BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429 is a medical device that received FDA 510(k) clearance on 1999-01-28. The listed applicant is Geiger Medical Technologies, Inc.. The 510(k) number is K983852.

When did BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429 receive FDA 510(k) clearance?

BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429 received FDA 510(k) clearance on 1999-01-28, under 510(k) number K983852.

Who is the listed applicant for BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429?

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 BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429?

The FDA product code for BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429 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.