SIGMA PROCEDURE #890
K-Number: K811784 · 1981-07-27
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Device Summary
Frequently Asked Questions
What is the SIGMA PROCEDURE #890?
SIGMA PROCEDURE #890 is a medical device that received FDA 510(k) clearance on 1981-07-27. The listed applicant is Sigma Chemical Co.. The 510(k) number is K811784.
When did SIGMA PROCEDURE #890 receive FDA 510(k) clearance?
SIGMA PROCEDURE #890 received FDA 510(k) clearance on 1981-07-27, under 510(k) number K811784.
Who is the listed applicant for SIGMA PROCEDURE #890?
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 SIGMA PROCEDURE #890?
The FDA product code for SIGMA PROCEDURE #890 is GJS.
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: GJS)
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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