F-12 MEDIUM, COON'S MODIFICATION PRODUCT NO. F6636
K-Number: K870529 · 1987-03-30
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Device Summary
Frequently Asked Questions
What is the F-12 MEDIUM, COON'S MODIFICATION PRODUCT NO. F6636?
F-12 MEDIUM, COON'S MODIFICATION PRODUCT NO. F6636 is a medical device that received FDA 510(k) clearance on 1987-03-30. The listed applicant is Sigma Chemical Co.. The 510(k) number is K870529.
When did F-12 MEDIUM, COON'S MODIFICATION PRODUCT NO. F6636 receive FDA 510(k) clearance?
F-12 MEDIUM, COON'S MODIFICATION PRODUCT NO. F6636 received FDA 510(k) clearance on 1987-03-30, under 510(k) number K870529.
Who is the listed applicant for F-12 MEDIUM, COON'S MODIFICATION PRODUCT NO. F6636?
The FDA 510(k) record lists Sigma Chemical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for F-12 MEDIUM, COON'S MODIFICATION PRODUCT NO. F6636?
The FDA product code for F-12 MEDIUM, COON'S MODIFICATION PRODUCT NO. F6636 is KIT.
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 Sigma Chemical Co. 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: KIT)
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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