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FDA 510(k)

MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE

K-Number: K925594 · 1993-02-12

ApplicantTri W-G, Inc.
Decision Date1993-02-12
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Tri W-G, Inc.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K925594. 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 MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE?

MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Tri W-G, Inc.. The 510(k) number is K925594.

When did MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE receive FDA 510(k) clearance?

MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE received FDA 510(k) clearance on 1993-02-12, under 510(k) number K925594.

Who is the listed applicant for MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE?

The FDA 510(k) record lists Tri W-G, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE?

The FDA product code for MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE is INQ.

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Other records listing Tri W-G, 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.

K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777K945163ECHOCARDIOGRAPHYK941720MODEL 747 AND 747-30 EXAM/TREATMENT TABLEK936303TREATMENT TABLE MODIFICATIONK933119HI-LO TREATMENT TABLESK932746MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE

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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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