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FDA 510(k)

WHITE SEALING CAP

K-Number: K791915 · 1979-12-19

ApplicantQuinton, Inc.
Decision Date1979-12-19
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WHITE SEALING CAP is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1979-12-19 under 510(k) number K791915. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHITE SEALING CAP?

WHITE SEALING CAP is a medical device that received FDA 510(k) clearance on 1979-12-19. The listed applicant is Quinton, Inc.. The 510(k) number is K791915.

When did WHITE SEALING CAP receive FDA 510(k) clearance?

WHITE SEALING CAP received FDA 510(k) clearance on 1979-12-19, under 510(k) number K791915.

Who is the listed applicant for WHITE SEALING CAP?

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

What is the FDA product code for WHITE SEALING CAP?

The FDA product code for WHITE SEALING CAP is DQO.

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Related Devices (Code: DQO)

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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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