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FDA 510(k)

SAFE-CONNECT I.V. EXTENSION SET

K-Number: K970524 · 1997-04-22

Decision Date1997-04-22
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFE-CONNECT I.V. EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Faulding Medical Device Co.. It received FDA 510(k) clearance on 1997-04-22 under 510(k) number K970524. 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 SAFE-CONNECT I.V. EXTENSION SET?

SAFE-CONNECT I.V. EXTENSION SET is a medical device that received FDA 510(k) clearance on 1997-04-22. The listed applicant is Faulding Medical Device Co.. The 510(k) number is K970524.

When did SAFE-CONNECT I.V. EXTENSION SET receive FDA 510(k) clearance?

SAFE-CONNECT I.V. EXTENSION SET received FDA 510(k) clearance on 1997-04-22, under 510(k) number K970524.

Who is the listed applicant for SAFE-CONNECT I.V. EXTENSION SET?

The FDA 510(k) record lists Faulding Medical Device Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFE-CONNECT I.V. EXTENSION SET?

The FDA product code for SAFE-CONNECT I.V. EXTENSION 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.

Other records listing Faulding Medical Device Co. 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.

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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