TUBULAR BANDAGE
K-Number: K802789 · 1980-12-10
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Device Summary
Frequently Asked Questions
What is the TUBULAR BANDAGE?
TUBULAR BANDAGE is a medical device that received FDA 510(k) clearance on 1980-12-10. The listed applicant is Secol Co.. The 510(k) number is K802789.
When did TUBULAR BANDAGE receive FDA 510(k) clearance?
TUBULAR BANDAGE received FDA 510(k) clearance on 1980-12-10, under 510(k) number K802789.
Who is the listed applicant for TUBULAR BANDAGE?
The FDA 510(k) record lists Secol Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBULAR BANDAGE?
The FDA product code for TUBULAR BANDAGE is FQM.
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 Secol 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: FQM)
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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