FDA 510(k)

3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE

K-Number: K934333 · 1994-07-07

Decision Date1994-07-07

Product CodeDRX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is 3M Medical Products Group. It received FDA 510(k) clearance on 1994-07-07 under 510(k) number K934333. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE?

3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-07-07. The listed applicant is 3M Medical Products Group. The 510(k) number is K934333.

When did 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE receive FDA 510(k) clearance?

3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE received FDA 510(k) clearance on 1994-07-07, under 510(k) number K934333.

Who is the listed applicant for 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE?

The FDA 510(k) record lists 3M Medical Products Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE?

The FDA product code for 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE is DRX.

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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.