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FDA 510(k)

RICH-MAR SPINA-MOBILIZOR

K-Number: K861832 · 1986-06-27

ApplicantRich-Mar Corp.
Decision Date1986-06-27
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RICH-MAR SPINA-MOBILIZOR 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 1986-06-27 under 510(k) number K861832. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICH-MAR SPINA-MOBILIZOR?

RICH-MAR SPINA-MOBILIZOR is a medical device that received FDA 510(k) clearance on 1986-06-27. The listed applicant is Rich-Mar Corp.. The 510(k) number is K861832.

When did RICH-MAR SPINA-MOBILIZOR receive FDA 510(k) clearance?

RICH-MAR SPINA-MOBILIZOR received FDA 510(k) clearance on 1986-06-27, under 510(k) number K861832.

Who is the listed applicant for RICH-MAR SPINA-MOBILIZOR?

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 RICH-MAR SPINA-MOBILIZOR?

The FDA product code for RICH-MAR SPINA-MOBILIZOR is ITH.

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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: ITH)

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.

K243775True Non-Surgical Spinal Decompression System (DRX9000-SL)Excite Medical of Tampa Bay, LLCK243366DRX9000C-SL Cervical Spinal Decompression SystemExcite Medical of Tampa Bay, LLCK214037Ergo-Flex Technologies Back on Trac (BOTGEN1) and Cervi-TracErgo-Flex Technologies, LLCK222912c1TracZimmer Medizinsysteme GmbHK112074EVERYWAY TRACTION UNIT, MODEL EVER-TRAC ET-800Everyway Medical Instruments Co.,LtdK103248INTEGRITY SPINAL CARE SYSTEMIntegra Life Sciences

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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