ULTRABRONZ SERIES 400 TANNING BED
K-Number: K931660 · 1993-12-17
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Device Summary
Frequently Asked Questions
What is the ULTRABRONZ SERIES 400 TANNING BED?
ULTRABRONZ SERIES 400 TANNING BED is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is Eurocut, Ltd.. The 510(k) number is K931660.
When did ULTRABRONZ SERIES 400 TANNING BED receive FDA 510(k) clearance?
ULTRABRONZ SERIES 400 TANNING BED received FDA 510(k) clearance on 1993-12-17, under 510(k) number K931660.
Who is the listed applicant for ULTRABRONZ SERIES 400 TANNING BED?
The FDA 510(k) record lists Eurocut, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRABRONZ SERIES 400 TANNING BED?
The FDA product code for ULTRABRONZ SERIES 400 TANNING BED is LEJ.
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 Eurocut, 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: LEJ)
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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