STRAP EASE 400
K-Number: K803063 · 1980-12-22
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Device Summary
Frequently Asked Questions
What is the STRAP EASE 400?
STRAP EASE 400 is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Independent Transfer Equipment Co.. The 510(k) number is K803063.
When did STRAP EASE 400 receive FDA 510(k) clearance?
STRAP EASE 400 received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803063.
Who is the listed applicant for STRAP EASE 400?
The FDA 510(k) record lists Independent Transfer Equipment Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRAP EASE 400?
The FDA product code for STRAP EASE 400 is ILK.
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 Independent Transfer Equipment 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: ILK)
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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