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FDA 510(k)

MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET

K-Number: K042234 · 2004-09-08

Decision Date2004-09-08
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Specialty Health Products, Inc.. It received FDA 510(k) clearance on 2004-09-08 under 510(k) number K042234. 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 MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET?

MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET is a medical device that received FDA 510(k) clearance on 2004-09-08. The listed applicant is Specialty Health Products, Inc.. The 510(k) number is K042234.

When did MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET receive FDA 510(k) clearance?

MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET received FDA 510(k) clearance on 2004-09-08, under 510(k) number K042234.

Who is the listed applicant for MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET?

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

What is the FDA product code for MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET?

The FDA product code for MODIFICATION TO: LIFTLOC SAFTEY 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.

Other records listing Specialty Health Products, 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.

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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