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FDA 510(k)

FT MODEL TABLE W/ELECTRIC HI LO OPTION E

K-Number: K925563 · 1993-05-26

ApplicantPro Med Mfg., Inc.
Decision Date1993-05-26
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FT MODEL TABLE W/ELECTRIC HI LO OPTION E is the device name listed in this FDA 510(k) record. The listed applicant is Pro Med Mfg., Inc.. It received FDA 510(k) clearance on 1993-05-26 under 510(k) number K925563. 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 FT MODEL TABLE W/ELECTRIC HI LO OPTION E?

FT MODEL TABLE W/ELECTRIC HI LO OPTION E is a medical device that received FDA 510(k) clearance on 1993-05-26. The listed applicant is Pro Med Mfg., Inc.. The 510(k) number is K925563.

When did FT MODEL TABLE W/ELECTRIC HI LO OPTION E receive FDA 510(k) clearance?

FT MODEL TABLE W/ELECTRIC HI LO OPTION E received FDA 510(k) clearance on 1993-05-26, under 510(k) number K925563.

Who is the listed applicant for FT MODEL TABLE W/ELECTRIC HI LO OPTION E?

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

What is the FDA product code for FT MODEL TABLE W/ELECTRIC HI LO OPTION E?

The FDA product code for FT MODEL TABLE W/ELECTRIC HI LO OPTION E is INQ.

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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

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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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