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FDA 510(k)

MORSE ANESTHESIA MANIFOLD

K-Number: K921322 · 1993-07-09

ApplicantNamic
Decision Date1993-07-09
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MORSE ANESTHESIA MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Namic. It received FDA 510(k) clearance on 1993-07-09 under 510(k) number K921322. 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 MORSE ANESTHESIA MANIFOLD?

MORSE ANESTHESIA MANIFOLD is a medical device that received FDA 510(k) clearance on 1993-07-09. The listed applicant is Namic. The 510(k) number is K921322.

When did MORSE ANESTHESIA MANIFOLD receive FDA 510(k) clearance?

MORSE ANESTHESIA MANIFOLD received FDA 510(k) clearance on 1993-07-09, under 510(k) number K921322.

Who is the listed applicant for MORSE ANESTHESIA MANIFOLD?

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

What is the FDA product code for MORSE ANESTHESIA MANIFOLD?

The FDA product code for MORSE ANESTHESIA MANIFOLD is FPA.

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Other records listing Namic 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.

K953676BREEZE DIGITAL INFLATION DEVICEK951722PERCEPTOR COMPENSATOR MORSE MANIFOLDK822100HIGH PRESSURE CONTRAST INJECTION LINEK813549CONTINUOUS FLUSH DEVICEK790082ARTERIAL EXTENSION SETK790083CATHETER, ARTERIAL LINE

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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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