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FDA 510(k)

TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777

K-Number: K960196 · 1996-02-07

ApplicantTri W-G, Inc.
Decision Date1996-02-07
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 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 1996-02-07 under 510(k) number K960196. 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 TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777?

TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 is a medical device that received FDA 510(k) clearance on 1996-02-07. The listed applicant is Tri W-G, Inc.. The 510(k) number is K960196.

When did TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 receive FDA 510(k) clearance?

TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 received FDA 510(k) clearance on 1996-02-07, under 510(k) number K960196.

Who is the listed applicant for TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777?

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 TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777?

The FDA product code for TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 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.

K945163ECHOCARDIOGRAPHYK941720MODEL 747 AND 747-30 EXAM/TREATMENT TABLEK936303TREATMENT TABLE MODIFICATIONK933119HI-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.K953621EVT-3300U.S. Table, Inc.K953622PTT 6200 ELEVATION THERAPY TABLEU.S. Table, Inc.K952357THE HILL ADJUSTABLE PODIATRY MODELHill Laboratories Co.

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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