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FDA 510(k)

LASER LAPARAXOPE

K-Number: K831241 · 1983-06-10

ApplicantEder Instrument Co, Inc.
Decision Date1983-06-10
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LASER LAPARAXOPE 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 1983-06-10 under 510(k) number K831241. 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 LASER LAPARAXOPE?

LASER LAPARAXOPE is a medical device that received FDA 510(k) clearance on 1983-06-10. The listed applicant is Eder Instrument Co, Inc.. The 510(k) number is K831241.

When did LASER LAPARAXOPE receive FDA 510(k) clearance?

LASER LAPARAXOPE received FDA 510(k) clearance on 1983-06-10, under 510(k) number K831241.

Who is the listed applicant for LASER LAPARAXOPE?

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

What is the FDA product code for LASER LAPARAXOPE?

The FDA product code for LASER LAPARAXOPE is HET.

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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 & PROBESK843499ARTHROSCOPY LEG HOLDERK831255LARYNGOSCOPE ATTACHMENT PH2000K831240LASER BRONCHOSCOPEK822959ENDOSCOPIC VIDEOSYSTEM

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Related Devices (Code: 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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