FDA 510(k) Premarket Notification K934333: 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE

Submission Details & Decision

Normalized public record details for 510(k) notification K934333.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K934333

Applicant / Sponsor

3M Medical Products Group

Device Name

3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE

Product Code

DRX

Decision Date

1994-07-07

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Traditional

Third Party Flag

Date Received

1993-09-07

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