ALARM SYS FOR NITROUS OXIDE SYS.
K-Number: K771246 · 1977-07-15
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Device Summary
Frequently Asked Questions
What is the ALARM SYS FOR NITROUS OXIDE SYS.?
ALARM SYS FOR NITROUS OXIDE SYS. is a medical device that received FDA 510(k) clearance on 1977-07-15. The listed applicant is Star Dental Mfg. Co.. The 510(k) number is K771246.
When did ALARM SYS FOR NITROUS OXIDE SYS. receive FDA 510(k) clearance?
ALARM SYS FOR NITROUS OXIDE SYS. received FDA 510(k) clearance on 1977-07-15, under 510(k) number K771246.
Who is the listed applicant for ALARM SYS FOR NITROUS OXIDE SYS.?
The FDA 510(k) record lists Star Dental Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALARM SYS FOR NITROUS OXIDE SYS.?
The FDA product code for ALARM SYS FOR NITROUS OXIDE SYS. is ECX.
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 Star Dental Mfg. Co. 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: ECX)
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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