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

MODEL 8-B WITH LA-2B ATTACHMENT FOR OB-GYN USE

K Number: K861845 · Decision Aug 11, 1986
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
47
Applicant Total
39
Review Days
90

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Basic Information

Device Name
MODEL 8-B WITH LA-2B ATTACHMENT FOR OB-GYN USE
K Number
K861845
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4550
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Directed Energy, Inc.
Date Received
May 13, 1986
Decision Date
August 11, 1986
Product Code
HHR
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
HHR Laser, Surgical, Gynecologic

Similar 510(k) Clearances

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Other Clearances by Directed Energy, Inc.

K Number Device Name
K904930 SURGICAL CARBON DIOXIDE LASER SYST MODEL 20-CH
K894241 MODEL 20-CH W/ AR-10A/U OPTICAL ATTACHMENT
K883738 CARBON DIOXIDE LASER SYSTEM MODEL 20-CX W/ATTACH.
K882926 MODEL AU-1 ACCESSORY UNIT
K880216 MODEL 20C W/AN AR-10A/U & RL-20A/U FOR ARTHROSCOP.
K873331 ORTHO. GAS INSUFFLATOR MODEL IN-2 FOR ARTHRO. SURG
K870841 MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.0 OB/GYN
K872709 MODEL 20-C, RL-20A/U, OB-10A/U
K872711 MODEL 20-C W/AR-10A/U ATTACH. FOR ARTHRO. SURGERY
K872710 MODEL 20-B W/OB-10A/U ATTACH. FOR EAR, NOSE/THROAT
Search all 39 clearances from Directed Energy, Inc. →