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FDA 510(k)

PORTABLE LIFT SEAT

K-Number: K923804 · 1993-02-12

ApplicantFrank H. Speckhart, P.E.
Decision Date1993-02-12
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PORTABLE LIFT SEAT is the device name listed in this FDA 510(k) record. The listed applicant is Frank H. Speckhart, P.E.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K923804. 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 PORTABLE LIFT SEAT?

PORTABLE LIFT SEAT is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Frank H. Speckhart, P.E.. The 510(k) number is K923804.

When did PORTABLE LIFT SEAT receive FDA 510(k) clearance?

PORTABLE LIFT SEAT received FDA 510(k) clearance on 1993-02-12, under 510(k) number K923804.

Who is the listed applicant for PORTABLE LIFT SEAT?

The FDA 510(k) record lists Frank H. Speckhart, P.E. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE LIFT SEAT?

The FDA product code for PORTABLE LIFT SEAT is INO.

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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.

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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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