ClearanceBrief
Company ยท US

Circon Acmi

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 2002. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)4
CCWLaryngoscope, Rigid1
FFKLithotriptor, Electro-Hydraulic1
GCJLaparoscope, General & Plastic Surgery1
HIFInsufflator, Laparoscopic1
HIGInsufflator, Hysteroscopic1
ODCEndoscope Channel Accessory1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 18, 2002K013165USA SERIES LAPAROSCOPES
Circon Acmi
GCJ
Nov 17, 1998K980492AEH-3 ELECTROHYDRAULIC LITHOTRIPTER AND PROBES (E-1F, E-3F, E-5F, AND E-9F)
Circon Acmi
FFK
Feb 28, 1991K905706GYN-1500 HYSTEROSCOPIC INUFFLATOR
Circon Acmi
HIG
Feb 28, 1991K905705LAP 3501 HIGH FLOW INSUFFLATOR
Circon Acmi
HIF
Apr 17, 1989K884097MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES
Circon Acmi
ODC
Mar 3, 1989K884025CIRCON ACMI BICAP II THERAPEUTIC SYSTEM BC-200
Circon Acmi
KNS
Jan 11, 1989K884254CIRCON ACMI BICAP III THERAPEUTIC SYSTEM
Circon Acmi
KNS
Jan 10, 1989K884252CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20
Circon Acmi
KNS
Jan 5, 1989K884306BICAP ABLATING FORCEPS BAF-7
Circon Acmi
KNS
Oct 17, 1988K883819BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P
Circon Acmi
CCW

Latest recalls

DateFirm and productCodeLinked 510(k)
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