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FDA 510(k)

GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS

K-Number: K935709 · 1994-01-31

ApplicantZimmer Patient Care Division
Decision Date1994-01-31
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Patient Care Division. It received FDA 510(k) clearance on 1994-01-31 under 510(k) number K935709. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS?

GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS is a medical device that received FDA 510(k) clearance on 1994-01-31. The listed applicant is Zimmer Patient Care Division. The 510(k) number is K935709.

When did GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS receive FDA 510(k) clearance?

GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS received FDA 510(k) clearance on 1994-01-31, under 510(k) number K935709.

Who is the listed applicant for GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS?

The FDA 510(k) record lists Zimmer Patient Care Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS?

The FDA product code for GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS is GCJ.

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Related Devices (Code: GCJ)

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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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