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FDA 510(k)

ABBOTT TESTPACK PLUS HCG URINE

K-Number: K894408 · 1989-09-05

Decision Date1989-09-05
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ABBOTT TESTPACK PLUS HCG URINE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1989-09-05 under 510(k) number K894408. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABBOTT TESTPACK PLUS HCG URINE?

ABBOTT TESTPACK PLUS HCG URINE is a medical device that received FDA 510(k) clearance on 1989-09-05. The listed applicant is Abbott Laboratories. The 510(k) number is K894408.

When did ABBOTT TESTPACK PLUS HCG URINE receive FDA 510(k) clearance?

ABBOTT TESTPACK PLUS HCG URINE received FDA 510(k) clearance on 1989-09-05, under 510(k) number K894408.

Who is the listed applicant for ABBOTT TESTPACK PLUS HCG URINE?

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 TESTPACK PLUS HCG URINE?

The FDA product code for ABBOTT TESTPACK PLUS HCG URINE is JHI.

Related Clinical Trials

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.

Other records listing Abbott Laboratories as applicant

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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Related Devices (Code: JHI)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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