GLIDE DEVICE
K-Number: K131870 · 2013-08-14
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Device Summary
Frequently Asked Questions
What is the GLIDE DEVICE?
GLIDE DEVICE is a medical device that received FDA 510(k) clearance on 2013-08-14. The listed applicant is Home Skinovations , Ltd.. The 510(k) number is K131870.
When did GLIDE DEVICE receive FDA 510(k) clearance?
GLIDE DEVICE received FDA 510(k) clearance on 2013-08-14, under 510(k) number K131870.
Who is the listed applicant for GLIDE DEVICE?
The FDA 510(k) record lists Home Skinovations , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLIDE DEVICE?
The FDA product code for GLIDE DEVICE is OHT.
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 Home Skinovations , Ltd. 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: OHT)
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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