ClearanceBrief
Company ยท US

Rnk Products, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2013. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DQDStethoscope, Electronic6

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 11, 2013K132560PCP-USB STETHOSCOPE
Rnk Products, Inc.
DQD
Oct 11, 2013K132405PPA/BT-RB STETHOSCOPE
Rnk Products, Inc.
DQD
Jan 20, 2011K102893PCP/PC STETHOSCOPE
Rnk Products, Inc.
DQD
Jun 6, 2008K081032TR-USB TELEPHONIC STETHOSCOPE
Rnk Products, Inc.
DQD
Oct 26, 2007K072026RNK ELECTRONIC STETHOSCOPE
Rnk Products, Inc.
DQD
Mar 10, 2004K034046RNK TELEPHONIC STETHOSCOPE, MODEL TR-1
Rnk Products
DQD

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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