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FDA 510(k)

DONWAY LIFTING FRAME

K-Number: K851660 · 1985-08-07

Decision Date1985-08-07
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DONWAY LIFTING FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Australian Biomedical Corporation , Ltd.. It received FDA 510(k) clearance on 1985-08-07 under 510(k) number K851660. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DONWAY LIFTING FRAME?

DONWAY LIFTING FRAME is a medical device that received FDA 510(k) clearance on 1985-08-07. The listed applicant is Australian Biomedical Corporation , Ltd.. The 510(k) number is K851660.

When did DONWAY LIFTING FRAME receive FDA 510(k) clearance?

DONWAY LIFTING FRAME received FDA 510(k) clearance on 1985-08-07, under 510(k) number K851660.

Who is the listed applicant for DONWAY LIFTING FRAME?

The FDA 510(k) record lists Australian Biomedical Corporation , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DONWAY LIFTING FRAME?

The FDA product code for DONWAY LIFTING FRAME is FPP.

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 Australian Biomedical Corporation , Ltd. 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: FPP)

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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