URIHESIVE STRIPS
K-Number: K802173 · 1980-09-26
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Device Summary
Frequently Asked Questions
What is the URIHESIVE STRIPS?
URIHESIVE STRIPS is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is E. R. Squibb & Sons, Inc.. The 510(k) number is K802173.
When did URIHESIVE STRIPS receive FDA 510(k) clearance?
URIHESIVE STRIPS received FDA 510(k) clearance on 1980-09-26, under 510(k) number K802173.
Who is the listed applicant for URIHESIVE STRIPS?
The FDA 510(k) record lists E. R. Squibb & Sons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URIHESIVE STRIPS?
The FDA product code for URIHESIVE STRIPS is KNX.
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 E. R. Squibb & Sons, 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: KNX)
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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