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FDA 510(k)

MANAN CONTRAST MEDIA ADMINISTRATION SET

K-Number: K864405 · 1986-12-18

ApplicantManan Manufacturing Co., Inc.
Decision Date1986-12-18
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MANAN CONTRAST MEDIA ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Manan Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1986-12-18 under 510(k) number K864405. 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 MANAN CONTRAST MEDIA ADMINISTRATION SET?

MANAN CONTRAST MEDIA ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1986-12-18. The listed applicant is Manan Manufacturing Co., Inc.. The 510(k) number is K864405.

When did MANAN CONTRAST MEDIA ADMINISTRATION SET receive FDA 510(k) clearance?

MANAN CONTRAST MEDIA ADMINISTRATION SET received FDA 510(k) clearance on 1986-12-18, under 510(k) number K864405.

Who is the listed applicant for MANAN CONTRAST MEDIA ADMINISTRATION SET?

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

What is the FDA product code for MANAN CONTRAST MEDIA ADMINISTRATION SET?

The FDA product code for MANAN CONTRAST MEDIA ADMINISTRATION SET is FPA.

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Other records listing Manan Manufacturing Co., Inc. as applicant

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.

K873208MANAN TURNER STYLE NEEDLEK863848MANAN BREST TUMOR LOCALIZATION NEEDLEK852018ARTHROGRAM TRAY FOR DOUBLE & SINGLE CONTRAST ARTHRK851832NAMAN POTTS COURNAND NEEDLEK852501MYELOGRAM PROCEDURE TRAYK851834MANAN GWI GUIDE WIRE INTRODUCER

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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

View on FDA Database →

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

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