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FDA 510(k)

COROMETRICS MEDICAL SYSTEMS 220 PH SYS.

K-Number: K800271 · 1980-02-26

ApplicantTransidyne General Corp.
Decision Date1980-02-26
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COROMETRICS MEDICAL SYSTEMS 220 PH SYS. is the device name listed in this FDA 510(k) record. The listed applicant is Transidyne General Corp.. It received FDA 510(k) clearance on 1980-02-26 under 510(k) number K800271. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COROMETRICS MEDICAL SYSTEMS 220 PH SYS.?

COROMETRICS MEDICAL SYSTEMS 220 PH SYS. is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Transidyne General Corp.. The 510(k) number is K800271.

When did COROMETRICS MEDICAL SYSTEMS 220 PH SYS. receive FDA 510(k) clearance?

COROMETRICS MEDICAL SYSTEMS 220 PH SYS. received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800271.

Who is the listed applicant for COROMETRICS MEDICAL SYSTEMS 220 PH SYS.?

The FDA 510(k) record lists Transidyne General Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COROMETRICS MEDICAL SYSTEMS 220 PH SYS.?

The FDA product code for COROMETRICS MEDICAL SYSTEMS 220 PH SYS. is CHL.

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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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