NON-STERILE GAUZE ROLLER BANDAGES
K-Number: K852265 · 1985-06-18
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Device Summary
Frequently Asked Questions
What is the NON-STERILE GAUZE ROLLER BANDAGES?
NON-STERILE GAUZE ROLLER BANDAGES is a medical device that received FDA 510(k) clearance on 1985-06-18. The listed applicant is Leonard Joseph Co.. The 510(k) number is K852265.
When did NON-STERILE GAUZE ROLLER BANDAGES receive FDA 510(k) clearance?
NON-STERILE GAUZE ROLLER BANDAGES received FDA 510(k) clearance on 1985-06-18, under 510(k) number K852265.
Who is the listed applicant for NON-STERILE GAUZE ROLLER BANDAGES?
The FDA 510(k) record lists Leonard Joseph Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-STERILE GAUZE ROLLER BANDAGES?
The FDA product code for NON-STERILE GAUZE ROLLER BANDAGES is EFQ.
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 Leonard Joseph 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: EFQ)
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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