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FDA 510(k)

TROCAR AND CANNULA ACCESSORY

K-Number: K945741 · 1995-02-28

ApplicantApplied Medical Resources
Decision Date1995-02-28
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROCAR AND CANNULA ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources. It received FDA 510(k) clearance on 1995-02-28 under 510(k) number K945741. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROCAR AND CANNULA ACCESSORY?

TROCAR AND CANNULA ACCESSORY is a medical device that received FDA 510(k) clearance on 1995-02-28. The listed applicant is Applied Medical Resources. The 510(k) number is K945741.

When did TROCAR AND CANNULA ACCESSORY receive FDA 510(k) clearance?

TROCAR AND CANNULA ACCESSORY received FDA 510(k) clearance on 1995-02-28, under 510(k) number K945741.

Who is the listed applicant for TROCAR AND CANNULA ACCESSORY?

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

What is the FDA product code for TROCAR AND CANNULA ACCESSORY?

The FDA product code for TROCAR AND CANNULA ACCESSORY is HET.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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