P-300 CAPNOGRAPH AND PULSE OXIMETER
K-Number: K915773 · 1992-06-24
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Device Summary
Frequently Asked Questions
What is the P-300 CAPNOGRAPH AND PULSE OXIMETER?
P-300 CAPNOGRAPH AND PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1992-06-24. The listed applicant is Pryon Corp.. The 510(k) number is K915773.
When did P-300 CAPNOGRAPH AND PULSE OXIMETER receive FDA 510(k) clearance?
P-300 CAPNOGRAPH AND PULSE OXIMETER received FDA 510(k) clearance on 1992-06-24, under 510(k) number K915773.
Who is the listed applicant for P-300 CAPNOGRAPH AND PULSE OXIMETER?
The FDA 510(k) record lists Pryon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for P-300 CAPNOGRAPH AND PULSE OXIMETER?
The FDA product code for P-300 CAPNOGRAPH AND PULSE OXIMETER is DQA.
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 Pryon Corp. 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: DQA)
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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