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FDA 510(k)

TMR-670

K-Number: K931349 · 1993-07-22

Decision Date1993-07-22
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TMR-670 is the device name listed in this FDA 510(k) record. The listed applicant is Pride Health Care, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K931349. The device is classified under product code INO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TMR-670?

TMR-670 is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Pride Health Care, Inc.. The 510(k) number is K931349.

When did TMR-670 receive FDA 510(k) clearance?

TMR-670 received FDA 510(k) clearance on 1993-07-22, under 510(k) number K931349.

Who is the listed applicant for TMR-670?

The FDA 510(k) record lists Pride Health Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TMR-670?

The FDA product code for TMR-670 is INO.

Other records listing Pride Health Care, 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.

View all 19 devices →

Related Devices (Code: INO)

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.

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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