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FDA 510(k)

ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE)

K-Number: K954336 · 1995-11-13

ApplicantAust & Taylor Medical Corp.
Decision Date1995-11-13
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE) is the device name listed in this FDA 510(k) record. The listed applicant is Aust & Taylor Medical Corp.. It received FDA 510(k) clearance on 1995-11-13 under 510(k) number K954336. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE)?

ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE) is a medical device that received FDA 510(k) clearance on 1995-11-13. The listed applicant is Aust & Taylor Medical Corp.. The 510(k) number is K954336.

When did ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE) receive FDA 510(k) clearance?

ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE) received FDA 510(k) clearance on 1995-11-13, under 510(k) number K954336.

Who is the listed applicant for ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE)?

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

What is the FDA product code for ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE)?

The FDA product code for ENDO-BEND GRASPER (114.3 MM SHAFT-STERILE) is EOB.

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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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