TCPM II TOURNIQUET CUFF PRESSURE MONITOR
K-Number: K900104 · 1990-03-15
Advertisement
Device Summary
Frequently Asked Questions
What is the TCPM II TOURNIQUET CUFF PRESSURE MONITOR?
TCPM II TOURNIQUET CUFF PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1990-03-15. The listed applicant is Electromedics, Inc.. The 510(k) number is K900104.
When did TCPM II TOURNIQUET CUFF PRESSURE MONITOR receive FDA 510(k) clearance?
TCPM II TOURNIQUET CUFF PRESSURE MONITOR received FDA 510(k) clearance on 1990-03-15, under 510(k) number K900104.
Who is the listed applicant for TCPM II TOURNIQUET CUFF PRESSURE MONITOR?
The FDA 510(k) record lists Electromedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TCPM II TOURNIQUET CUFF PRESSURE MONITOR?
The FDA product code for TCPM II TOURNIQUET CUFF PRESSURE MONITOR is KCY.
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 Electromedics, Inc. 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: KCY)
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