CERALAS DIODE LASER SYSTEM (CERALAS D2)
K-Number: K964751 · 1997-02-21
Advertisement
Device Summary
Frequently Asked Questions
What is the CERALAS DIODE LASER SYSTEM (CERALAS D2)?
CERALAS DIODE LASER SYSTEM (CERALAS D2) is a medical device that received FDA 510(k) clearance on 1997-02-21. The listed applicant is Ceram Optec, Inc.. The 510(k) number is K964751.
When did CERALAS DIODE LASER SYSTEM (CERALAS D2) receive FDA 510(k) clearance?
CERALAS DIODE LASER SYSTEM (CERALAS D2) received FDA 510(k) clearance on 1997-02-21, under 510(k) number K964751.
Who is the listed applicant for CERALAS DIODE LASER SYSTEM (CERALAS D2)?
The FDA 510(k) record lists Ceram Optec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CERALAS DIODE LASER SYSTEM (CERALAS D2)?
The FDA product code for CERALAS DIODE LASER SYSTEM (CERALAS D2) is HQF.
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 Ceram Optec, 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: HQF)
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.
Advertisement