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FDA 510(k)

HASSON 360 SERIES ENDOSCOPIC GRASPING FORCEPS

K-Number: K934451 · 1994-03-17

ApplicantCook Urological, Inc.
Decision Date1994-03-17
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HASSON 360 SERIES ENDOSCOPIC GRASPING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Cook Urological, Inc.. It received FDA 510(k) clearance on 1994-03-17 under 510(k) number K934451. 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 360 SERIES ENDOSCOPIC GRASPING FORCEPS?

HASSON 360 SERIES ENDOSCOPIC GRASPING FORCEPS is a medical device that received FDA 510(k) clearance on 1994-03-17. The listed applicant is Cook Urological, Inc.. The 510(k) number is K934451.

When did HASSON 360 SERIES ENDOSCOPIC GRASPING FORCEPS receive FDA 510(k) clearance?

HASSON 360 SERIES ENDOSCOPIC GRASPING FORCEPS received FDA 510(k) clearance on 1994-03-17, under 510(k) number K934451.

Who is the listed applicant for HASSON 360 SERIES ENDOSCOPIC GRASPING FORCEPS?

The FDA 510(k) record lists Cook Urological, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HASSON 360 SERIES ENDOSCOPIC GRASPING FORCEPS?

The FDA product code for HASSON 360 SERIES ENDOSCOPIC GRASPING FORCEPS 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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