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FDA 510(k)

MULTIPLE NEEDLE, INJECTION, DISPOSABLE

K-Number: K872566 · 1987-08-25

ApplicantCotran Corp.
Decision Date1987-08-25
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTIPLE NEEDLE, INJECTION, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Cotran Corp.. It received FDA 510(k) clearance on 1987-08-25 under 510(k) number K872566. 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 MULTIPLE NEEDLE, INJECTION, DISPOSABLE?

MULTIPLE NEEDLE, INJECTION, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1987-08-25. The listed applicant is Cotran Corp.. The 510(k) number is K872566.

When did MULTIPLE NEEDLE, INJECTION, DISPOSABLE receive FDA 510(k) clearance?

MULTIPLE NEEDLE, INJECTION, DISPOSABLE received FDA 510(k) clearance on 1987-08-25, under 510(k) number K872566.

Who is the listed applicant for MULTIPLE NEEDLE, INJECTION, DISPOSABLE?

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

What is the FDA product code for MULTIPLE NEEDLE, INJECTION, DISPOSABLE?

The FDA product code for MULTIPLE NEEDLE, INJECTION, DISPOSABLE 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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