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FDA 510(k)

PROMEDICOR

K-Number: K863514 · 1986-09-25

Decision Date1986-09-25
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROMEDICOR is the device name listed in this FDA 510(k) record. The listed applicant is Terra Marketing Assoc.. It received FDA 510(k) clearance on 1986-09-25 under 510(k) number K863514. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROMEDICOR?

PROMEDICOR is a medical device that received FDA 510(k) clearance on 1986-09-25. The listed applicant is Terra Marketing Assoc.. The 510(k) number is K863514.

When did PROMEDICOR receive FDA 510(k) clearance?

PROMEDICOR received FDA 510(k) clearance on 1986-09-25, under 510(k) number K863514.

Who is the listed applicant for PROMEDICOR?

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

What is the FDA product code for PROMEDICOR?

The FDA product code for PROMEDICOR is FMI.

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: FMI)

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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