SURGICUTT - BLEEDING TIME DEVICE
K-Number: K850542 · 1985-03-01
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Device Summary
Frequently Asked Questions
What is the SURGICUTT - BLEEDING TIME DEVICE?
SURGICUTT - BLEEDING TIME DEVICE is a medical device that received FDA 510(k) clearance on 1985-03-01. The listed applicant is International Technidyne Corp.. The 510(k) number is K850542.
When did SURGICUTT - BLEEDING TIME DEVICE receive FDA 510(k) clearance?
SURGICUTT - BLEEDING TIME DEVICE received FDA 510(k) clearance on 1985-03-01, under 510(k) number K850542.
Who is the listed applicant for SURGICUTT - BLEEDING TIME DEVICE?
The FDA 510(k) record lists International Technidyne Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGICUTT - BLEEDING TIME DEVICE?
The FDA product code for SURGICUTT - BLEEDING TIME DEVICE is JCA.
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 International Technidyne 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: JCA)
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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