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FDA 510(k)

NITROGLYCERIN I.V. ADMINISTRATION SET

K-Number: K833939 · 1984-02-21

ApplicantCritikon Company, LLC
Decision Date1984-02-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NITROGLYCERIN I.V. ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Critikon Company, LLC. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K833939. 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 NITROGLYCERIN I.V. ADMINISTRATION SET?

NITROGLYCERIN I.V. ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Critikon Company, LLC. The 510(k) number is K833939.

When did NITROGLYCERIN I.V. ADMINISTRATION SET receive FDA 510(k) clearance?

NITROGLYCERIN I.V. ADMINISTRATION SET received FDA 510(k) clearance on 1984-02-21, under 510(k) number K833939.

Who is the listed applicant for NITROGLYCERIN I.V. ADMINISTRATION SET?

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

What is the FDA product code for NITROGLYCERIN I.V. ADMINISTRATION SET?

The FDA product code for NITROGLYCERIN I.V. ADMINISTRATION SET is FPA.

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Other records listing Critikon Company, LLC as applicant

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K002248DINAMAP PRO 1000 MONITOR, MODEL 1000K000500DINAMAP ADVANCED NIBP MODULEK992638DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400K982342DINAMAP MPS SELECT PORTABLE MONITORK943709DINAMAP PLUS VITAL SIGNS MONOITORK942700DINAMAP VITAL SIGNS MONITOR MODELS 9300 AND 9320/9340

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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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