SURGIPRESS SURGICAL LOOP
K-Number: K843593 · 1984-10-24
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Device Summary
Frequently Asked Questions
What is the SURGIPRESS SURGICAL LOOP?
SURGIPRESS SURGICAL LOOP is a medical device that received FDA 510(k) clearance on 1984-10-24. The listed applicant is Syntex Corp.. The 510(k) number is K843593.
When did SURGIPRESS SURGICAL LOOP receive FDA 510(k) clearance?
SURGIPRESS SURGICAL LOOP received FDA 510(k) clearance on 1984-10-24, under 510(k) number K843593.
Who is the listed applicant for SURGIPRESS SURGICAL LOOP?
The FDA 510(k) record lists Syntex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGIPRESS SURGICAL LOOP?
The FDA product code for SURGIPRESS SURGICAL LOOP is HRQ.
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 Syntex 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: HRQ)
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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