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FDA 510(k)

HASSON OPEN LAPAROSCOPY CANNULA

K-Number: K942447 · 1994-12-15

ApplicantLinvatec Corp.
Decision Date1994-12-15
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HASSON OPEN LAPAROSCOPY CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Linvatec Corp.. It received FDA 510(k) clearance on 1994-12-15 under 510(k) number K942447. 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 HASSON OPEN LAPAROSCOPY CANNULA?

HASSON OPEN LAPAROSCOPY CANNULA is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Linvatec Corp.. The 510(k) number is K942447.

When did HASSON OPEN LAPAROSCOPY CANNULA receive FDA 510(k) clearance?

HASSON OPEN LAPAROSCOPY CANNULA received FDA 510(k) clearance on 1994-12-15, under 510(k) number K942447.

Who is the listed applicant for HASSON OPEN LAPAROSCOPY CANNULA?

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

What is the FDA product code for HASSON OPEN LAPAROSCOPY CANNULA?

The FDA product code for HASSON OPEN LAPAROSCOPY CANNULA 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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