FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CABOT FIBER LASER PROBE

K Number: K873115 · Decision Jan 28, 1988
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
38
Review Days
171

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Basic Information

Device Name
CABOT FIBER LASER PROBE
K Number
K873115
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Cabot Medical Corp.
Date Received
August 10, 1987
Decision Date
January 28, 1988
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

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Other Clearances by Cabot Medical Corp.

K Number Device Name
K960148 CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENT
K946109 CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPS
K951972 CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHS
K951714 CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBER
K941743 CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP
K934115 3000 ELECTRONIC INSUFFLATOR MODIFICATION
K932293 CABOT MEDICAL BIPOLAR CUTTING FORCEPS
K930954 THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV
K932626 CABOT MEDICAL SURGIFLEX(R) SUCTION-IRRIGATION PROB
K935786 CORSON AND NEZHAT SUCTION/IRRIGATION PROBES
Search all 38 clearances from Cabot Medical Corp. →