MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP
K-Number: K860342 · 1986-03-04
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Device Summary
Frequently Asked Questions
What is the MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP?
MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP is a medical device that received FDA 510(k) clearance on 1986-03-04. The listed applicant is Bio/Data Corp.. The 510(k) number is K860342.
When did MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP receive FDA 510(k) clearance?
MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP received FDA 510(k) clearance on 1986-03-04, under 510(k) number K860342.
Who is the listed applicant for MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP?
The FDA 510(k) record lists Bio/Data Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP?
The FDA product code for MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP is JPA.
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 Bio/Data Corp. 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: JPA)
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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