Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES

K-Number: K971444 · 1997-06-11

Decision Date1997-06-11
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES 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 1997-06-11 under 510(k) number K971444. 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 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES?

3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES is a medical device that received FDA 510(k) clearance on 1997-06-11. The listed applicant is 3M Medical Products Group. The 510(k) number is K971444.

When did 3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES receive FDA 510(k) clearance?

3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES received FDA 510(k) clearance on 1997-06-11, under 510(k) number K971444.

Who is the listed applicant for 3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES?

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 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES?

The FDA product code for 3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES is DRX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing 3M Medical Products Group as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 12 devices →

Related Devices (Code: DRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑