FDA 510(k)

INTRA-ARTICULATED EDGER-PLANER SYSTEM

K-Number: K792353 · 1979-12-27

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date1979-12-27

Product CodeHWE

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

INTRA-ARTICULATED EDGER-PLANER SYSTEM 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 1979-12-27 under 510(k) number K792353. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRA-ARTICULATED EDGER-PLANER SYSTEM?

INTRA-ARTICULATED EDGER-PLANER SYSTEM is a medical device that received FDA 510(k) clearance on 1979-12-27. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K792353.

When did INTRA-ARTICULATED EDGER-PLANER SYSTEM receive FDA 510(k) clearance?

INTRA-ARTICULATED EDGER-PLANER SYSTEM received FDA 510(k) clearance on 1979-12-27, under 510(k) number K792353.

Who is the listed applicant for INTRA-ARTICULATED EDGER-PLANER SYSTEM?

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 INTRA-ARTICULATED EDGER-PLANER SYSTEM?

The FDA product code for INTRA-ARTICULATED EDGER-PLANER SYSTEM is HWE.

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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.