ALPHA CHUCK
K-Number: K853970 · 1985-11-08
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Device Summary
Frequently Asked Questions
What is the ALPHA CHUCK?
ALPHA CHUCK is a medical device that received FDA 510(k) clearance on 1985-11-08. The listed applicant is Rocky Mountain Medical Corp.. The 510(k) number is K853970.
When did ALPHA CHUCK receive FDA 510(k) clearance?
ALPHA CHUCK received FDA 510(k) clearance on 1985-11-08, under 510(k) number K853970.
Who is the listed applicant for ALPHA CHUCK?
The FDA 510(k) record lists Rocky Mountain Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALPHA CHUCK?
The FDA product code for ALPHA CHUCK is KME.
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 Rocky Mountain Medical Corp. 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: KME)
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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