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FDA 510(k)

LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG

K-Number: K953584 · 1995-10-24

ApplicantAbbott Laboratories
Decision Date1995-10-24
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1995-10-24 under 510(k) number K953584. 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 LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG?

LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG is a medical device that received FDA 510(k) clearance on 1995-10-24. The listed applicant is Abbott Laboratories. The 510(k) number is K953584.

When did LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG receive FDA 510(k) clearance?

LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG received FDA 510(k) clearance on 1995-10-24, under 510(k) number K953584.

Who is the listed applicant for LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG?

The FDA product code for LIFESHIELD LUER ACTIVATED VALVE MALE ADAPTER PLUG is FPA.

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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.

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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.

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