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FDA 510(k)

DUOFLO DISPENSER

K-Number: K872565 · 1987-12-29

ApplicantHemaedics, Inc.
Decision Date1987-12-29
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUOFLO DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Hemaedics, Inc.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K872565. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUOFLO DISPENSER?

DUOFLO DISPENSER is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Hemaedics, Inc.. The 510(k) number is K872565.

When did DUOFLO DISPENSER receive FDA 510(k) clearance?

DUOFLO DISPENSER received FDA 510(k) clearance on 1987-12-29, under 510(k) number K872565.

Who is the listed applicant for DUOFLO DISPENSER?

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

What is the FDA product code for DUOFLO DISPENSER?

The FDA product code for DUOFLO DISPENSER is FMF.

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Related Devices (Code: FMF)

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.

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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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