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FDA 510(k)

MICRO INFUSION SET

K-Number: K833949 · 1984-01-11

ApplicantDeltec Systems, Inc.
Decision Date1984-01-11
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICRO INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Deltec Systems, Inc.. It received FDA 510(k) clearance on 1984-01-11 under 510(k) number K833949. 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 MICRO INFUSION SET?

MICRO INFUSION SET is a medical device that received FDA 510(k) clearance on 1984-01-11. The listed applicant is Deltec Systems, Inc.. The 510(k) number is K833949.

When did MICRO INFUSION SET receive FDA 510(k) clearance?

MICRO INFUSION SET received FDA 510(k) clearance on 1984-01-11, under 510(k) number K833949.

Who is the listed applicant for MICRO INFUSION SET?

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

What is the FDA product code for MICRO INFUSION SET?

The FDA product code for MICRO INFUSION SET is FPA.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Deltec Systems, 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.

K871132PHARMACIA DELTEC SUBCLAVIAN INTRODUCERSK870768AC ADAPTER ACCESSORY, PRODUCT CODE 600123AK862927CADD-1, MODEL 5100 HFK854964CADD-LD 5500 AMBU INFUSION PUMP&3010 10ML MED RES.K853584CADD-1, MODEL 5100 HF, AMBULATORY INFUSION PUMPK850183CADD-VT, 5300 AMBULATORY INFUSION PUMP W/3050, 50M

View all 9 devices →

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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