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FDA 510(k)

PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE

K-Number: K942046 · 1994-10-04

Decision Date1994-10-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE 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 1994-10-04 under 510(k) number K942046. 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 PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE?

PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K942046.

When did PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE receive FDA 510(k) clearance?

PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE received FDA 510(k) clearance on 1994-10-04, under 510(k) number K942046.

Who is the listed applicant for PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE?

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 EXTENSION SET WITH ANTI-SIPHON VALVE?

The FDA product code for PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE 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.

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: 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.

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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