7200 MICROPROCESS VENT SYS/MODEL 7202 DISPLAY OPT
K-Number: K862604 · 1986-08-01
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Device Summary
Frequently Asked Questions
What is the 7200 MICROPROCESS VENT SYS/MODEL 7202 DISPLAY OPT?
7200 MICROPROCESS VENT SYS/MODEL 7202 DISPLAY OPT is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K862604.
When did 7200 MICROPROCESS VENT SYS/MODEL 7202 DISPLAY OPT receive FDA 510(k) clearance?
7200 MICROPROCESS VENT SYS/MODEL 7202 DISPLAY OPT received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862604.
Who is the listed applicant for 7200 MICROPROCESS VENT SYS/MODEL 7202 DISPLAY OPT?
The FDA 510(k) record lists Puritan Bennett Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 7200 MICROPROCESS VENT SYS/MODEL 7202 DISPLAY OPT?
The FDA product code for 7200 MICROPROCESS VENT SYS/MODEL 7202 DISPLAY OPT 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 Puritan Bennett 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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