LASTOBAND ADHESIVE BANDAGES
K-Number: K831454 · 1983-10-31
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Device Summary
Frequently Asked Questions
What is the LASTOBAND ADHESIVE BANDAGES?
LASTOBAND ADHESIVE BANDAGES is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K831454.
When did LASTOBAND ADHESIVE BANDAGES receive FDA 510(k) clearance?
LASTOBAND ADHESIVE BANDAGES received FDA 510(k) clearance on 1983-10-31, under 510(k) number K831454.
Who is the listed applicant for LASTOBAND ADHESIVE BANDAGES?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LASTOBAND ADHESIVE BANDAGES?
The FDA product code for LASTOBAND ADHESIVE BANDAGES is NAD.
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 Smith & Nephew, Inc. 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: NAD)
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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