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FDA 510(k)

QUIK LOK

K-Number: K840878 · 1984-03-30

ApplicantAbbott Laboratories
Decision Date1984-03-30
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

QUIK LOK is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K840878. 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 QUIK LOK?

QUIK LOK is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Abbott Laboratories. The 510(k) number is K840878.

When did QUIK LOK receive FDA 510(k) clearance?

QUIK LOK received FDA 510(k) clearance on 1984-03-30, under 510(k) number K840878.

Who is the listed applicant for QUIK LOK?

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 QUIK LOK?

The FDA product code for QUIK LOK 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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