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FDA 510(k)

QUICK-CHECK

K-Number: K790277 · 1979-03-16

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1979-03-16
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUICK-CHECK is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1979-03-16 under 510(k) number K790277. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK-CHECK?

QUICK-CHECK is a medical device that received FDA 510(k) clearance on 1979-03-16. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K790277.

When did QUICK-CHECK receive FDA 510(k) clearance?

QUICK-CHECK received FDA 510(k) clearance on 1979-03-16, under 510(k) number K790277.

Who is the listed applicant for QUICK-CHECK?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUICK-CHECK?

The FDA product code for QUICK-CHECK is DXN.

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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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