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FDA 510(k)

DISSECTION PROBE

K-Number: K955163 · 1996-01-24

ApplicantOrigin Medsystems, Inc.
Decision Date1996-01-24
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISSECTION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1996-01-24 under 510(k) number K955163. 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 DISSECTION PROBE?

DISSECTION PROBE is a medical device that received FDA 510(k) clearance on 1996-01-24. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K955163.

When did DISSECTION PROBE receive FDA 510(k) clearance?

DISSECTION PROBE received FDA 510(k) clearance on 1996-01-24, under 510(k) number K955163.

Who is the listed applicant for DISSECTION PROBE?

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

What is the FDA product code for DISSECTION PROBE?

The FDA product code for DISSECTION PROBE 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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