MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM
K-Number: K800650 · 1980-04-02
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Device Summary
Frequently Asked Questions
What is the MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM?
MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is Hospal Medical Corp.. The 510(k) number is K800650.
When did MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM receive FDA 510(k) clearance?
MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800650.
Who is the listed applicant for MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM?
The FDA 510(k) record lists Hospal Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM?
The FDA product code for MOD. 300 ANESTH. VOL. VENTILATOR W/ALARM is CBK.
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 Hospal Medical 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: CBK)
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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