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FDA 510(k)

MICROS(TM)

K-Number: K871995 · 1987-10-23

ApplicantControlled Release Technologies, Inc.
Decision Date1987-10-23
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROS(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Controlled Release Technologies, Inc.. It received FDA 510(k) clearance on 1987-10-23 under 510(k) number K871995. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROS(TM)?

MICROS(TM) is a medical device that received FDA 510(k) clearance on 1987-10-23. The listed applicant is Controlled Release Technologies, Inc.. The 510(k) number is K871995.

When did MICROS(TM) receive FDA 510(k) clearance?

MICROS(TM) received FDA 510(k) clearance on 1987-10-23, under 510(k) number K871995.

Who is the listed applicant for MICROS(TM)?

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

What is the FDA product code for MICROS(TM)?

The FDA product code for MICROS(TM) is FPA.

Related Clinical Trials

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Related Devices (Code: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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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