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FDA 510(k)

TREATMENT TABLE MODIFICATION

K-Number: K936303 · 1994-03-18

ApplicantTri W-G, Inc.
Decision Date1994-03-18
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TREATMENT TABLE MODIFICATION 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 1994-03-18 under 510(k) number K936303. 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 TREATMENT TABLE MODIFICATION?

TREATMENT TABLE MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-03-18. The listed applicant is Tri W-G, Inc.. The 510(k) number is K936303.

When did TREATMENT TABLE MODIFICATION receive FDA 510(k) clearance?

TREATMENT TABLE MODIFICATION received FDA 510(k) clearance on 1994-03-18, under 510(k) number K936303.

Who is the listed applicant for TREATMENT TABLE MODIFICATION?

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 TREATMENT TABLE MODIFICATION?

The FDA product code for TREATMENT TABLE MODIFICATION 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 TABLEK933119HI-LO TREATMENT TABLESK932746MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLEK930802MODELS 642 & 643 TILT EXAM/TREATMENT 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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