TOE LOOPS
K-Number: K780194 · 1978-02-14
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Device Summary
Frequently Asked Questions
What is the TOE LOOPS?
TOE LOOPS is a medical device that received FDA 510(k) clearance on 1978-02-14. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K780194.
When did TOE LOOPS receive FDA 510(k) clearance?
TOE LOOPS received FDA 510(k) clearance on 1978-02-14, under 510(k) number K780194.
Who is the listed applicant for TOE LOOPS?
The FDA 510(k) record lists Orthopedic Equipment Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TOE LOOPS?
The FDA product code for TOE LOOPS is KNO.
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 Orthopedic Equipment Co., 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: KNO)
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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