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FDA 510(k)

GEIGER NEEDLE ADAPTER, MODEL 406

K-Number: K001029 · 2000-05-23

ApplicantGeiger Medical Technologies, Inc.
Decision Date2000-05-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GEIGER NEEDLE ADAPTER, MODEL 406 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 2000-05-23 under 510(k) number K001029. 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 NEEDLE ADAPTER, MODEL 406?

GEIGER NEEDLE ADAPTER, MODEL 406 is a medical device that received FDA 510(k) clearance on 2000-05-23. The listed applicant is Geiger Medical Technologies, Inc.. The 510(k) number is K001029.

When did GEIGER NEEDLE ADAPTER, MODEL 406 receive FDA 510(k) clearance?

GEIGER NEEDLE ADAPTER, MODEL 406 received FDA 510(k) clearance on 2000-05-23, under 510(k) number K001029.

Who is the listed applicant for GEIGER NEEDLE ADAPTER, MODEL 406?

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 NEEDLE ADAPTER, MODEL 406?

The FDA product code for GEIGER NEEDLE ADAPTER, MODEL 406 is GEI.

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Other records listing Geiger Medical Technologies, Inc. as applicant

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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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