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FDA 510(k)

OPERATING TABLES & AMPLINOX 03

K-Number: K792569 · 1980-01-04

Decision Date1980-01-04
Product CodeBWN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OPERATING TABLES & AMPLINOX 03 is the device name listed in this FDA 510(k) record. The listed applicant is Ets Rene Marzet. It received FDA 510(k) clearance on 1980-01-04 under 510(k) number K792569. The device is classified under product code BWN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPERATING TABLES & AMPLINOX 03?

OPERATING TABLES & AMPLINOX 03 is a medical device that received FDA 510(k) clearance on 1980-01-04. The listed applicant is Ets Rene Marzet. The 510(k) number is K792569.

When did OPERATING TABLES & AMPLINOX 03 receive FDA 510(k) clearance?

OPERATING TABLES & AMPLINOX 03 received FDA 510(k) clearance on 1980-01-04, under 510(k) number K792569.

Who is the listed applicant for OPERATING TABLES & AMPLINOX 03?

The FDA 510(k) record lists Ets Rene Marzet as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPERATING TABLES & AMPLINOX 03?

The FDA product code for OPERATING TABLES & AMPLINOX 03 is BWN.

Related Clinical Trials

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.

Other records listing Ets Rene Marzet 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.

Related Devices (Code: BWN)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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