Decision Date1980-05-23
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120 is the device name listed in this FDA 510(k) record. The listed applicant is R2 Corp.. It received FDA 510(k) clearance on 1980-05-23 under 510(k) number K800932. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120?
ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120 is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is R2 Corp.. The 510(k) number is K800932.
When did ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120 receive FDA 510(k) clearance?
ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120 received FDA 510(k) clearance on 1980-05-23, under 510(k) number K800932.
Who is the listed applicant for ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120?
The FDA 510(k) record lists R2 Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120?
The FDA product code for ECG-RF-CHOKE CABLE-ADAPTER #'S 121,120 is DSA.
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Official Source
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