Narco Tlecare Miniature Pressure Dome

FDA 510(k) K810431 · Narco Bio-Systems

Substantially Equivalent

510(k) numberK810431

Submission

Device name
Narco Tlecare Miniature Pressure Dome
Applicant
Narco Bio-Systems
Mchenry, IL, US
Received
February 19, 1981
Decision date
March 11, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DRS – Transducer, Blood-Pressure, Extravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2850
Specialty
Cardiovascular

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More from Mirador Biomedical

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K832869Motility Measurement Sys MMS-100FFX · Traditional 10/31/1983SE
K813502Narco Telecare Isoflo Pressure MonitorDRS · Traditional 12/29/1981SE
K811376Ultrasonic QFM System 1000DPW · Traditional 08/13/1981SE
K801544Porta-Fib LPDLDD · Traditional 07/14/1980SE
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Questions and answers

When was Narco Tlecare Miniature Pressure Dome cleared by the FDA?

Narco Tlecare Miniature Pressure Dome (K810431) received a 510(k) decision of Substantially Equivalent on March 11, 1981, 20 days after the submission was received.

What is the product code of K810431?

The FDA product code is DRS – Transducer, Blood-Pressure, Extravascular, a Class II (moderate risk) device regulated under 21 CFR 870.2850.