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FDA 510(k)

30 IV EXTENSION SET W/TWO MALE LUER LOCKS

K-Number: K882503 · 1988-08-25

ApplicantChurchill Medical Systems, Inc.
Decision Date1988-08-25
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

30 IV EXTENSION SET W/TWO MALE LUER LOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Medical Systems, Inc.. It received FDA 510(k) clearance on 1988-08-25 under 510(k) number K882503. 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 30 IV EXTENSION SET W/TWO MALE LUER LOCKS?

30 IV EXTENSION SET W/TWO MALE LUER LOCKS is a medical device that received FDA 510(k) clearance on 1988-08-25. The listed applicant is Churchill Medical Systems, Inc.. The 510(k) number is K882503.

When did 30 IV EXTENSION SET W/TWO MALE LUER LOCKS receive FDA 510(k) clearance?

30 IV EXTENSION SET W/TWO MALE LUER LOCKS received FDA 510(k) clearance on 1988-08-25, under 510(k) number K882503.

Who is the listed applicant for 30 IV EXTENSION SET W/TWO MALE LUER LOCKS?

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

What is the FDA product code for 30 IV EXTENSION SET W/TWO MALE LUER LOCKS?

The FDA product code for 30 IV EXTENSION SET W/TWO MALE LUER LOCKS 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 Churchill Medical 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.

K041038CHURCHILL MEDICAL DUAL CHAMBER EMPTY CONTAINERK021395MODIFICATION TO 30 EXTENSION SETK013949UNIVERSAL VIAL ACCESS SPIKE WITH NEEDLELESS CONNECTORK020544WING SAFE INFUSION SET 20 GA, SHS2000 SERIES; WING SAFE INFUSION SET 19 GA, SHS1900 SERIES; WING SAFE INFUSION SET 22 GAK013950VENTED VIAL ACCESS DEVICEK012157CHURCHILL MEDICAL SYSTEMS STOPCOCK

View all 12 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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