FDA 510(k)

STRYKER STRYKEFLOW ELECTROCAUTERY PROBES

K-Number: K963765 · 1997-01-31

Decision Date1997-01-31

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STRYKER STRYKEFLOW ELECTROCAUTERY PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 1997-01-31 under 510(k) number K963765. 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 STRYKER STRYKEFLOW ELECTROCAUTERY PROBES?

STRYKER STRYKEFLOW ELECTROCAUTERY PROBES is a medical device that received FDA 510(k) clearance on 1997-01-31. The listed applicant is Stryker Endoscopy. The 510(k) number is K963765.

When did STRYKER STRYKEFLOW ELECTROCAUTERY PROBES receive FDA 510(k) clearance?

STRYKER STRYKEFLOW ELECTROCAUTERY PROBES received FDA 510(k) clearance on 1997-01-31, under 510(k) number K963765.

Who is the listed applicant for STRYKER STRYKEFLOW ELECTROCAUTERY PROBES?

The FDA 510(k) record lists Stryker Endoscopy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRYKER STRYKEFLOW ELECTROCAUTERY PROBES?

The FDA product code for STRYKER STRYKEFLOW ELECTROCAUTERY PROBES 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.