ClearanceBrief
Company ยท US

The Urology Group

FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1984. 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
FZXGuide, Surgical, Instrument1
GEIElectrosurgical, Cutting & Coagulation & Accessories1
KNXCollector, Urine, (And Accessories) For Indwelling Catheter1
KQTEvacuator, Gastro-Urology1
NADDressing, Wound, Occlusive1
OCVEndoscope Holder1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 3, 1984K831703COVERUPS
The Urology Group
NAD
Dec 12, 1983K831489SURGICAL TUBE HOLDER
The Urology Group
GEI
Jun 26, 1981K810739SUCTION WOUND DRAINAGE DEVICE
The Urology Group
KQT
Apr 17, 1981K810788SURGICAL TUBE HOLDER
The Urology Group
FZX
Mar 31, 1981K810787UROLOGIC TUBE HOLDER
The Urology Group
OCV
Aug 12, 1980K801629COVER-ALL MALE INCONTINENCE DEVICE
The Urology Group
KNX

Latest recalls

DateFirm and productCodeLinked 510(k)
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