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FDA 510(k)

ASSIST-A-LIFT

K-Number: K881298 · 1988-04-21

Decision Date1988-04-21
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ASSIST-A-LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Action Engineering, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881298. The device is classified under product code INO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASSIST-A-LIFT?

ASSIST-A-LIFT is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Action Engineering, Inc.. The 510(k) number is K881298.

When did ASSIST-A-LIFT receive FDA 510(k) clearance?

ASSIST-A-LIFT received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881298.

Who is the listed applicant for ASSIST-A-LIFT?

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

What is the FDA product code for ASSIST-A-LIFT?

The FDA product code for ASSIST-A-LIFT is INO.

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.

Related Devices (Code: INO)

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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