Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SUBCUTANEOUS INFUSION SET

K-Number: K932637 · 1994-01-07

ApplicantDouglas Medical Products Corp.
Decision Date1994-01-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUBCUTANEOUS INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Douglas Medical Products Corp.. It received FDA 510(k) clearance on 1994-01-07 under 510(k) number K932637. 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 SUBCUTANEOUS INFUSION SET?

SUBCUTANEOUS INFUSION SET is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Douglas Medical Products Corp.. The 510(k) number is K932637.

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

SUBCUTANEOUS INFUSION SET received FDA 510(k) clearance on 1994-01-07, under 510(k) number K932637.

Who is the listed applicant for SUBCUTANEOUS INFUSION SET?

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

What is the FDA product code for SUBCUTANEOUS INFUSION SET?

The FDA product code for SUBCUTANEOUS 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 Douglas Medical Products Corp. 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.

K961155SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908K954428SOLOPICC 24 (60CM) 20GA CATHETERK94162840 MICRON BLOOD TRANSFUSION FILTERK9421014-LEAD IRRIGATION SETK941453CHECK VALVE SOLUTION SETK930854SOLUTION SET WITH .2 MICRON FILTER

View all 19 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.

↑