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FDA 510(k)

THERA-TRONIC THERAPEUTIC TREATMENT TABLE

K-Number: K852651 · 1985-09-30

ApplicantRwm Co.
Decision Date1985-09-30
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THERA-TRONIC THERAPEUTIC TREATMENT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Rwm Co.. It received FDA 510(k) clearance on 1985-09-30 under 510(k) number K852651. 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 THERA-TRONIC THERAPEUTIC TREATMENT TABLE?

THERA-TRONIC THERAPEUTIC TREATMENT TABLE is a medical device that received FDA 510(k) clearance on 1985-09-30. The listed applicant is Rwm Co.. The 510(k) number is K852651.

When did THERA-TRONIC THERAPEUTIC TREATMENT TABLE receive FDA 510(k) clearance?

THERA-TRONIC THERAPEUTIC TREATMENT TABLE received FDA 510(k) clearance on 1985-09-30, under 510(k) number K852651.

Who is the listed applicant for THERA-TRONIC THERAPEUTIC TREATMENT TABLE?

The FDA 510(k) record lists Rwm Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERA-TRONIC THERAPEUTIC TREATMENT TABLE?

The FDA product code for THERA-TRONIC THERAPEUTIC TREATMENT TABLE 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

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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