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FDA 510(k)

TATCH-IT

K-Number: K870356 · 1987-06-12

Decision Date1987-06-12
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TATCH-IT is the device name listed in this FDA 510(k) record. The listed applicant is Reunion Medical Co.. It received FDA 510(k) clearance on 1987-06-12 under 510(k) number K870356. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TATCH-IT?

TATCH-IT is a medical device that received FDA 510(k) clearance on 1987-06-12. The listed applicant is Reunion Medical Co.. The 510(k) number is K870356.

When did TATCH-IT receive FDA 510(k) clearance?

TATCH-IT received FDA 510(k) clearance on 1987-06-12, under 510(k) number K870356.

Who is the listed applicant for TATCH-IT?

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

What is the FDA product code for TATCH-IT?

The FDA product code for TATCH-IT is DRS.

Related Clinical Trials

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.

Related Devices (Code: DRS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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