PRIMARY SOLUTION ADMIN. SET-#86-01-0 260
K-Number: K801871 · 1980-08-27
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Device Summary
Frequently Asked Questions
What is the PRIMARY SOLUTION ADMIN. SET-#86-01-0 260?
PRIMARY SOLUTION ADMIN. SET-#86-01-0 260 is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Y. The 510(k) number is K801871.
When did PRIMARY SOLUTION ADMIN. SET-#86-01-0 260 receive FDA 510(k) clearance?
PRIMARY SOLUTION ADMIN. SET-#86-01-0 260 received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801871.
Who is the listed applicant for PRIMARY SOLUTION ADMIN. SET-#86-01-0 260?
The FDA 510(k) record lists Y as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRIMARY SOLUTION ADMIN. SET-#86-01-0 260?
The FDA product code for PRIMARY SOLUTION ADMIN. SET-#86-01-0 260 is FPA.
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 Y 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: FPA)
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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