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FDA 510(k)

MEDI-PLINTH

K-Number: K924905 · 1993-02-16

ApplicantMedi-Man Rehabilitation Products, Inc.
Decision Date1993-02-16
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDI-PLINTH is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Man Rehabilitation Products, Inc.. It received FDA 510(k) clearance on 1993-02-16 under 510(k) number K924905. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-PLINTH?

MEDI-PLINTH is a medical device that received FDA 510(k) clearance on 1993-02-16. The listed applicant is Medi-Man Rehabilitation Products, Inc.. The 510(k) number is K924905.

When did MEDI-PLINTH receive FDA 510(k) clearance?

MEDI-PLINTH received FDA 510(k) clearance on 1993-02-16, under 510(k) number K924905.

Who is the listed applicant for MEDI-PLINTH?

The FDA 510(k) record lists Medi-Man Rehabilitation Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-PLINTH?

The FDA product code for MEDI-PLINTH is INQ.

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Other records listing Medi-Man Rehabilitation Products, 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.

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Related Devices (Code: INQ)

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.

K960334CARDON PHYSICAL THERAPY TABLE MODEL R27116Cardon Rehabilitation Products, Inc.K960336CARDON PHYSICAL THERAPY TABLE MODEL R27645Cardon Rehabilitation Products, Inc.K960332CARDON PHYSICAL THERAPY TABLE MODEL R28598Cardon Rehabilitation Products, Inc.K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777Tri W-G, Inc.K953621EVT-3300U.S. Table, Inc.K953622PTT 6200 ELEVATION THERAPY TABLEU.S. Table, Inc.

Official Source

View on FDA Database →

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

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