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FDA 510(k)

LIFESHIELD ADDITIVE PIERCING PIN

K-Number: K002006 · 2000-08-10

ApplicantAbbott Laboratories
Decision Date2000-08-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFESHIELD ADDITIVE PIERCING PIN is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2000-08-10 under 510(k) number K002006. 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 ADDITIVE PIERCING PIN?

LIFESHIELD ADDITIVE PIERCING PIN is a medical device that received FDA 510(k) clearance on 2000-08-10. The listed applicant is Abbott Laboratories. The 510(k) number is K002006.

When did LIFESHIELD ADDITIVE PIERCING PIN receive FDA 510(k) clearance?

LIFESHIELD ADDITIVE PIERCING PIN received FDA 510(k) clearance on 2000-08-10, under 510(k) number K002006.

Who is the listed applicant for LIFESHIELD ADDITIVE PIERCING PIN?

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 ADDITIVE PIERCING PIN?

The FDA product code for LIFESHIELD ADDITIVE PIERCING PIN 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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