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FDA 510(k)

JACOB CHUCK

K-Number: K802694 · 1980-11-12

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1980-11-12
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

JACOB CHUCK is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802694. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JACOB CHUCK?

JACOB CHUCK is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K802694.

When did JACOB CHUCK receive FDA 510(k) clearance?

JACOB CHUCK received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802694.

Who is the listed applicant for JACOB CHUCK?

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

What is the FDA product code for JACOB CHUCK?

The FDA product code for JACOB CHUCK is LXH.

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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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