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FDA 510(k)

TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES

K-Number: K942389 · 1996-02-16

ApplicantHogan & Hartson
Decision Date1996-02-16
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1996-02-16 under 510(k) number K942389. 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 TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES?

TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES is a medical device that received FDA 510(k) clearance on 1996-02-16. The listed applicant is Hogan & Hartson. The 510(k) number is K942389.

When did TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES receive FDA 510(k) clearance?

TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES received FDA 510(k) clearance on 1996-02-16, under 510(k) number K942389.

Who is the listed applicant for TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES?

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

What is the FDA product code for TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES?

The FDA product code for TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES 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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