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FDA 510(k)

ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54)

K-Number: K894180 · 1989-09-13

ApplicantAbbott Laboratories
Decision Date1989-09-13
Product CodeCIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54) is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1989-09-13 under 510(k) number K894180. The device is classified under product code CIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54)?

ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54) is a medical device that received FDA 510(k) clearance on 1989-09-13. The listed applicant is Abbott Laboratories. The 510(k) number is K894180.

When did ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54) receive FDA 510(k) clearance?

ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54) received FDA 510(k) clearance on 1989-09-13, under 510(k) number K894180.

Who is the listed applicant for ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54)?

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 ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54)?

The FDA product code for ABBOTT AST-ACTIVATED (LIQUID, LIST#01A54) is CIT.

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Related Devices (Code: CIT)

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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