Ecg-Rf-Choke Cable-Adapter #'S 121,120

FDA 510(k) K800932 · R2 Corp.

Substantially Equivalent

510(k) numberK800932

Submission

Device name
Ecg-Rf-Choke Cable-Adapter #'S 121,120
Applicant
R2 Corp.
Mchenry, IL, US
Received
April 21, 1980
Decision date
May 23, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DSA – Cable, Transducer And Electrode, Patient, (Including Connector)
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2900
Specialty
Cardiovascular

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More from Baylis Medical Technologies, Inc.

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K800937R2 Plate Type Cable-Adaptor #S 175,176LDD · Traditional 05/23/1980SE
K800936R2 Paddle Type Cable-Adaptor #S 170,171LDD · Traditional 05/23/1980SE
K800935R2 Apex-Post.,Ant.&Post. ELECT.(12 Mods)DRX · Traditional 05/23/1980SE
K800931R2(TM) ECG Cable-Adaptor #'S 120-121-122DSA · Traditional 05/23/1980SE
K800930R2(TM) ECG Electrode SET-#'S305-306 Etc.DRX · Traditional 05/23/1980SE
K800934R2 Esu Cable-Adapter Models 160,161IKD · Traditional 05/20/1980SE
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Questions and answers

When was Ecg-Rf-Choke Cable-Adapter #'S 121,120 cleared by the FDA?

Ecg-Rf-Choke Cable-Adapter #'S 121,120 (K800932) received a 510(k) decision of Substantially Equivalent on May 23, 1980, 32 days after the submission was received.

What is the product code of K800932?

The FDA product code is DSA – Cable, Transducer And Electrode, Patient, (Including Connector), a Class II (moderate risk) device regulated under 21 CFR 870.2900.