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FDA 510(k)

TEST, SEROSONIC ALBUMIN

K-Number: K760355 · 1976-10-05

ApplicantMallinckrodt Critical Care
Decision Date1976-10-05
Product CodeCIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TEST, SEROSONIC ALBUMIN is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Critical Care. It received FDA 510(k) clearance on 1976-10-05 under 510(k) number K760355. The device is classified under product code CIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEST, SEROSONIC ALBUMIN?

TEST, SEROSONIC ALBUMIN is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Mallinckrodt Critical Care. The 510(k) number is K760355.

When did TEST, SEROSONIC ALBUMIN receive FDA 510(k) clearance?

TEST, SEROSONIC ALBUMIN received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760355.

Who is the listed applicant for TEST, SEROSONIC ALBUMIN?

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

What is the FDA product code for TEST, SEROSONIC ALBUMIN?

The FDA product code for TEST, SEROSONIC ALBUMIN is CIX.

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Related Devices (Code: CIX)

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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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