Tr-Usb Telephonic Stethoscope

FDA 510(k) K081032 · Rnk Products, Inc.

Substantially Equivalent

510(k) numberK081032

Submission

Device name
Tr-Usb Telephonic Stethoscope
Applicant
Rnk Products, Inc.
Burnsville, MN, US
Received
April 11, 2008
Decision date
June 6, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DQD – Stethoscope, Electronic
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1875
Specialty
Cardiovascular

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More from Sparrow Acoustics, Inc.

510(k)DeviceDecision
K132560Pcp-Usb StethoscopeDQD · Traditional 10/11/2013SE
K132405Ppa/Bt-Rb StethoscopeDQD · Traditional 10/11/2013SE
K102893Pcp/Pc StethoscopeDQD · Traditional 01/20/2011SE
K072026RNK Electronic StethoscopeDQD · Traditional 10/26/2007SE
K034046RNK Telephonic Stethoscope, Model TR-1DQD · Traditional 03/10/2004SE

Questions and answers

When was Tr-Usb Telephonic Stethoscope cleared by the FDA?

Tr-Usb Telephonic Stethoscope (K081032) received a 510(k) decision of Substantially Equivalent on June 6, 2008, 56 days after the submission was received.

What is the product code of K081032?

The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.