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)

PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS

K-Number: K932211 · 1994-05-02

Decision Date1994-05-02
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K932211. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS?

PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K932211.

When did PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS receive FDA 510(k) clearance?

PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS received FDA 510(k) clearance on 1994-05-02, under 510(k) number K932211.

Who is the listed applicant for PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS?

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

What is the FDA product code for PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS?

The FDA product code for PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS is LJS.

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.

Other records listing Pharmacia Deltec, 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.

View all 43 devices →

Related Devices (Code: LJS)

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.

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.

↑