SHAPE-ACTIO METAL TOXICOLOGY CONTROL
K-Number: K890721 · 1989-04-10
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Device Summary
Frequently Asked Questions
What is the SHAPE-ACTIO METAL TOXICOLOGY CONTROL?
SHAPE-ACTIO METAL TOXICOLOGY CONTROL is a medical device that received FDA 510(k) clearance on 1989-04-10. The listed applicant is Actio, Inc.. The 510(k) number is K890721.
When did SHAPE-ACTIO METAL TOXICOLOGY CONTROL receive FDA 510(k) clearance?
SHAPE-ACTIO METAL TOXICOLOGY CONTROL received FDA 510(k) clearance on 1989-04-10, under 510(k) number K890721.
Who is the listed applicant for SHAPE-ACTIO METAL TOXICOLOGY CONTROL?
The FDA 510(k) record lists Actio, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHAPE-ACTIO METAL TOXICOLOGY CONTROL?
The FDA product code for SHAPE-ACTIO METAL TOXICOLOGY CONTROL is DIE.
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 Actio, Inc. 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: DIE)
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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