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FDA 510(k)

SHARPE ENDONEEDLE HOLDER

K-Number: K920549 · 1992-09-22

ApplicantPaladin Medical, Inc.
Decision Date1992-09-22
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SHARPE ENDONEEDLE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Paladin Medical, Inc.. It received FDA 510(k) clearance on 1992-09-22 under 510(k) number K920549. 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 SHARPE ENDONEEDLE HOLDER?

SHARPE ENDONEEDLE HOLDER is a medical device that received FDA 510(k) clearance on 1992-09-22. The listed applicant is Paladin Medical, Inc.. The 510(k) number is K920549.

When did SHARPE ENDONEEDLE HOLDER receive FDA 510(k) clearance?

SHARPE ENDONEEDLE HOLDER received FDA 510(k) clearance on 1992-09-22, under 510(k) number K920549.

Who is the listed applicant for SHARPE ENDONEEDLE HOLDER?

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

What is the FDA product code for SHARPE ENDONEEDLE HOLDER?

The FDA product code for SHARPE ENDONEEDLE HOLDER 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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