8-WATT PULSED DENTAL LASER SYSTEM
K-Number: K930789 · 1993-05-21
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Device Summary
Frequently Asked Questions
What is the 8-WATT PULSED DENTAL LASER SYSTEM?
8-WATT PULSED DENTAL LASER SYSTEM is a medical device that received FDA 510(k) clearance on 1993-05-21. The listed applicant is Sunrise Technologies, Inc.. The 510(k) number is K930789.
When did 8-WATT PULSED DENTAL LASER SYSTEM receive FDA 510(k) clearance?
8-WATT PULSED DENTAL LASER SYSTEM received FDA 510(k) clearance on 1993-05-21, under 510(k) number K930789.
Who is the listed applicant for 8-WATT PULSED DENTAL LASER SYSTEM?
The FDA 510(k) record lists Sunrise Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 8-WATT PULSED DENTAL LASER SYSTEM?
The FDA product code for 8-WATT PULSED DENTAL LASER SYSTEM is GEX. This falls under the Gastroenterology category.
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 Sunrise Technologies, 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: GEX)
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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