MODEL 86-01-1 260 SOLUTION ADMIN. SET
K-Number: K801872 · 1980-08-27
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Device Summary
Frequently Asked Questions
What is the MODEL 86-01-1 260 SOLUTION ADMIN. SET?
MODEL 86-01-1 260 SOLUTION ADMIN. SET is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Y. The 510(k) number is K801872.
When did MODEL 86-01-1 260 SOLUTION ADMIN. SET receive FDA 510(k) clearance?
MODEL 86-01-1 260 SOLUTION ADMIN. SET received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801872.
Who is the listed applicant for MODEL 86-01-1 260 SOLUTION ADMIN. SET?
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 MODEL 86-01-1 260 SOLUTION ADMIN. SET?
The FDA product code for MODEL 86-01-1 260 SOLUTION ADMIN. SET 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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