RETRACTOR RODS
K-Number: K930032 · 1994-02-10
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Device Summary
Frequently Asked Questions
What is the RETRACTOR RODS?
RETRACTOR RODS is a medical device that received FDA 510(k) clearance on 1994-02-10. The listed applicant is Thomasville Medical Assoc.. The 510(k) number is K930032.
When did RETRACTOR RODS receive FDA 510(k) clearance?
RETRACTOR RODS received FDA 510(k) clearance on 1994-02-10, under 510(k) number K930032.
Who is the listed applicant for RETRACTOR RODS?
The FDA 510(k) record lists Thomasville Medical Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RETRACTOR RODS?
The FDA product code for RETRACTOR RODS is KNA.
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 Thomasville Medical Assoc. 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: KNA)
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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