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FDA 510(k)

PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH

K-Number: K932198 · 1994-05-02

Decision Date1994-05-02
Product CodeLJS
Advisory CommitteeHO
DecisionUnknown

Device Summary

PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH 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 K932198. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH?

PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH 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 K932198.

When did PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH receive FDA 510(k) clearance?

PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH received FDA 510(k) clearance on 1994-05-02, under 510(k) number K932198.

Who is the listed applicant for PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH?

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 PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH?

The FDA product code for PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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