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

SLIT LAMP ATTACHMENT

K Number: K801877 · Decision Sep 16, 1980
Classifications
1
FEI Numbers
26
Registration Numbers
27
Same Product Code
29
Applicant Total
32
Review Days
41

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Basic Information

Device Name
SLIT LAMP ATTACHMENT
K Number
K801877
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4690
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cavitron Corp.
Date Received
August 6, 1980
Decision Date
September 16, 1980
Product Code
HQB
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HQB Photocoagulator And Accessories

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Other Clearances by Cavitron Corp.

K Number Device Name
K811582 THE PLACER
K810207 MINOR SURGERY LIGHT
K802928 SPIROMETRIC COMPUTER #SC-10
K801623 CAVITRON ULTRASONIC SURG. ASPIR. CUSA
K800869 MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA
K800722 AUTO-FIELD D AUTOMATED VISUAL DETECTOR
K791585 MODEL G-61 ULTRASONIC DENTAL UNIT
K791277 MODEL 6500 EXTRACTION IRRIGATION SYS
K782054 LASER, CO2 SURGICAL
K782065 LASER, PHOTOCOAGULATION
Search all 32 clearances from Cavitron Corp. →