ACCUTORQ II
K-Number: K760929 · 1976-11-19
Advertisement
Device Summary
Frequently Asked Questions
What is the ACCUTORQ II?
ACCUTORQ II is a medical device that received FDA 510(k) clearance on 1976-11-19. The listed applicant is Ritter Co.. The 510(k) number is K760929.
When did ACCUTORQ II receive FDA 510(k) clearance?
ACCUTORQ II received FDA 510(k) clearance on 1976-11-19, under 510(k) number K760929.
Who is the listed applicant for ACCUTORQ II?
The FDA 510(k) record lists Ritter Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACCUTORQ II?
The FDA product code for ACCUTORQ II is EFB.
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 Ritter 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: EFB)
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.
Advertisement