ABBOTT TESTPACK PLUS TM HCG-COMBO
K-Number: K903219 · 1990-09-25
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Device Summary
Frequently Asked Questions
What is the ABBOTT TESTPACK PLUS TM HCG-COMBO?
ABBOTT TESTPACK PLUS TM HCG-COMBO is a medical device that received FDA 510(k) clearance on 1990-09-25. The listed applicant is Abbott Laboratories. The 510(k) number is K903219.
When did ABBOTT TESTPACK PLUS TM HCG-COMBO receive FDA 510(k) clearance?
ABBOTT TESTPACK PLUS TM HCG-COMBO received FDA 510(k) clearance on 1990-09-25, under 510(k) number K903219.
Who is the listed applicant for ABBOTT TESTPACK PLUS TM HCG-COMBO?
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 TM HCG-COMBO?
The FDA product code for ABBOTT TESTPACK PLUS TM HCG-COMBO 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.
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
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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