SUCTION RETRACTOR
K-Number: K875289 · 1988-01-22
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Device Summary
Frequently Asked Questions
What is the SUCTION RETRACTOR?
SUCTION RETRACTOR is a medical device that received FDA 510(k) clearance on 1988-01-22. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K875289.
When did SUCTION RETRACTOR receive FDA 510(k) clearance?
SUCTION RETRACTOR received FDA 510(k) clearance on 1988-01-22, under 510(k) number K875289.
Who is the listed applicant for SUCTION RETRACTOR?
The FDA 510(k) record lists T. Korossurgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUCTION RETRACTOR?
The FDA product code for SUCTION RETRACTOR is GAD.
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 T. Korossurgical Instruments 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: GAD)
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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