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FDA 510(k)

FILTER SYSTEM, ALTNER DISPOSABLE

K-Number: K790209 · 1979-02-26

Decision Date1979-02-26
Product CodeGAZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FILTER SYSTEM, ALTNER DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1979-02-26 under 510(k) number K790209. The device is classified under product code GAZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTER SYSTEM, ALTNER DISPOSABLE?

FILTER SYSTEM, ALTNER DISPOSABLE is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K790209.

When did FILTER SYSTEM, ALTNER DISPOSABLE receive FDA 510(k) clearance?

FILTER SYSTEM, ALTNER DISPOSABLE received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790209.

Who is the listed applicant for FILTER SYSTEM, ALTNER DISPOSABLE?

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

What is the FDA product code for FILTER SYSTEM, ALTNER DISPOSABLE?

The FDA product code for FILTER SYSTEM, ALTNER DISPOSABLE is GAZ.

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 Orthopedic Equipment 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.

View all 45 devices →

Related Devices (Code: GAZ)

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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