RED DOT 2269 INFANT MONITORING ELECTRODE
K-Number: K902080 · 1990-07-18
Advertisement
Device Summary
Frequently Asked Questions
What is the RED DOT 2269 INFANT MONITORING ELECTRODE?
RED DOT 2269 INFANT MONITORING ELECTRODE is a medical device that received FDA 510(k) clearance on 1990-07-18. The listed applicant is 3M Company. The 510(k) number is K902080.
When did RED DOT 2269 INFANT MONITORING ELECTRODE receive FDA 510(k) clearance?
RED DOT 2269 INFANT MONITORING ELECTRODE received FDA 510(k) clearance on 1990-07-18, under 510(k) number K902080.
Who is the listed applicant for RED DOT 2269 INFANT MONITORING ELECTRODE?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RED DOT 2269 INFANT MONITORING ELECTRODE?
The FDA product code for RED DOT 2269 INFANT MONITORING ELECTRODE 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 Company 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.
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.
Advertisement