ClearanceBrief
Company ยท US

Farrall Instruments, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1995. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LILMonitor, Penile Tumescence2
HCBDevice, Aversive Conditioning1
HCCDevice, Biofeedback1
HIRPerineometer1
LELDevice, Sleep Assessment1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 10, 1995K940128CAT-400UL PENILE PLETHYSMOGRAPH
Farrall Instruments, Inc.
LIL
Jan 10, 1995K936115CAT-600 PENILE PLETHYSMOGRAPH
Farrall Instruments, Inc.
LIL
Sep 15, 1982K821723BI-4520 DUAL IMPEDOMETER
Farrall Instruments, Inc.
Jul 13, 1982K821664PP-100, PERSONAL PERINEOMETER
Farrall Instruments, Inc.
HIR
Dec 20, 1979K792305A SLEEP ASSESSMENT DEVICE
Farrall Instruments, Inc.
LEL
Oct 3, 1978K781634VISUALAX
Farrall Instruments, Inc.
HCC
Jul 20, 1976K760166STIMULATOR, SONIC CONTROL (AS-1)
Farrall Instruments, Inc.
HCB

Latest recalls

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