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FDA 510(k)

ARTHROSCOPY LEG HOLDER

K-Number: K843499 · 1984-10-31

ApplicantEder Instrument Co, Inc.
Decision Date1984-10-31
Product Code
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPY LEG HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Eder Instrument Co, Inc.. It received FDA 510(k) clearance on 1984-10-31 under 510(k) number K843499. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPY LEG HOLDER?

ARTHROSCOPY LEG HOLDER is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is Eder Instrument Co, Inc.. The 510(k) number is K843499.

When did ARTHROSCOPY LEG HOLDER receive FDA 510(k) clearance?

ARTHROSCOPY LEG HOLDER received FDA 510(k) clearance on 1984-10-31, under 510(k) number K843499.

Who is the listed applicant for ARTHROSCOPY LEG HOLDER?

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

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Other records listing Eder Instrument Co, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K843498BIPOLAR SUCTION ELECTRODEK843497SURGICAL KNIVES & PROBESK831255LARYNGOSCOPE ATTACHMENT PH2000K831240LASER BRONCHOSCOPEK831241LASER LAPARAXOPEK822959ENDOSCOPIC VIDEOSYSTEM

View all 10 devices →

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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