ClearanceBrief
Company ยท US

Snowden-Pencer

FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 2003. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEIElectrosurgical, Cutting & Coagulation & Accessories3
HIFInsufflator, Laparoscopic3
GCJLaparoscope, General & Plastic Surgery2
FBMCannula And Trocar, Suprapubic, Non-Disposable1
HEIMonitor, Heart-Valve Movement, Fetal, Ultrasonic1
HFICoagulator, Culdoscopic (And Accessories)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 4, 2003K030890SWITCHBLADE
Snowden Pencer, Inc.
GEI
Mar 12, 1996K960400DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)
Snowden-Pencer
FBM
May 19, 1994K930666REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY
Snowden-Pencer
GEI
May 16, 1994K930667REUSABLE LAPAROSCOPIC INSTRUMENTS
Snowden-Pencer
GCJ
Feb 28, 1994K924148DIAMOND-SHARP(R) TROCARS
Snowden-Pencer
HFI
Jan 26, 1993K924149ENDO I/A PROBE
Snowden-Pencer
GCJ
Jun 9, 1992K920985SNOWDEN-PENCER IRRIGATION PUMP
Snowden-Pencer
HEI
Jun 4, 1992K920986SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700
Snowden-Pencer
HIF
Nov 27, 1991K913979ENDO I/A Y SET
Snowden-Pencer
HIF
Nov 7, 1991K913835SNOWDEN-PENCER INSUFFLATOR TUBING SET
Snowden-Pencer
HIF
Jun 19, 1986K861372ELECTROSURGICAL CUTTING AND COAGULATION ACCESSORY
Snowden-Pencer
GEI

Latest recalls

DateFirm and productCodeLinked 510(k)
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