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FDA 510(k)

HLE-1000 HIGH/LOW TREATMENT TABLE

K-Number: K883659 · 1988-10-13

ApplicantRich-Mar Corp.
Decision Date1988-10-13
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HLE-1000 HIGH/LOW TREATMENT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Rich-Mar Corp.. It received FDA 510(k) clearance on 1988-10-13 under 510(k) number K883659. 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 HLE-1000 HIGH/LOW TREATMENT TABLE?

HLE-1000 HIGH/LOW TREATMENT TABLE is a medical device that received FDA 510(k) clearance on 1988-10-13. The listed applicant is Rich-Mar Corp.. The 510(k) number is K883659.

When did HLE-1000 HIGH/LOW TREATMENT TABLE receive FDA 510(k) clearance?

HLE-1000 HIGH/LOW TREATMENT TABLE received FDA 510(k) clearance on 1988-10-13, under 510(k) number K883659.

Who is the listed applicant for HLE-1000 HIGH/LOW TREATMENT TABLE?

The FDA 510(k) record lists Rich-Mar Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HLE-1000 HIGH/LOW TREATMENT TABLE?

The FDA product code for HLE-1000 HIGH/LOW TREATMENT TABLE is INQ.

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Other records listing Rich-Mar Corp. 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.

K040679RICH-MAR AUTOPRISM INFRARED LAMPK031018AUTOGEL PADK032941AUTOSOUND 7.6 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICEK021483RICH-MAR THERASOUND 6.5 THERAPEUTIC ULTRASOUNDK013770MODIFICATION TO: WINNER ST-2 STIMULATORK013771MODIFICATION TO: WINNER CM-2 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICE

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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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