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FDA 510(k)

COAGULATING CANNULA DEVICE

K-Number: K953696 · 1995-12-08

ApplicantDorsal Orthopedic Corp.
Decision Date1995-12-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COAGULATING CANNULA DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Dorsal Orthopedic Corp.. It received FDA 510(k) clearance on 1995-12-08 under 510(k) number K953696. 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 COAGULATING CANNULA DEVICE?

COAGULATING CANNULA DEVICE is a medical device that received FDA 510(k) clearance on 1995-12-08. The listed applicant is Dorsal Orthopedic Corp.. The 510(k) number is K953696.

When did COAGULATING CANNULA DEVICE receive FDA 510(k) clearance?

COAGULATING CANNULA DEVICE received FDA 510(k) clearance on 1995-12-08, under 510(k) number K953696.

Who is the listed applicant for COAGULATING CANNULA DEVICE?

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

What is the FDA product code for COAGULATING CANNULA DEVICE?

The FDA product code for COAGULATING CANNULA DEVICE 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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