FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HAAG-STREIT SLIT LAMP 900

K Number: K792083 · Decision Nov 16, 1979
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
13
Applicant Total
43
Review Days
31

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HAAG-STREIT SLIT LAMP 900
K Number
K792083
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4700
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Lumenis, Inc.
Date Received
October 16, 1979
Decision Date
November 16, 1979
Product Code
HRM
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
HRM Microscope, Operating & Accessories, Ac-Powered, Ophthalmic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HRM), ordered by most recent decision date.

View all

Other Clearances by Lumenis, Inc.

K Number Device Name
K211979 Lumenis Y&R Laser System
K151109 Lumenis Smart532 Laser System
K130195 SCANNING LASERLINK
K111213 VISION ONE LASER SYSTEM
K100228 VERSAPULSE MODEL P20 LASER SYSTEM
K091962 POLYSCOPE FLEXIBLE ENDOSCOPY CATHETER; 10,000 PIXEL FIBER OPTIC; XENON LIGHT SOURCE, MODEL LS-200
K082809 ACUPULSE 30 AND 40 CARBON DIOXIDE LASER SYSTEM
K081704 SELECTA FAMILY OF OPHITHALMIC LASER SYSTEMS
K053628 LIGHTSHEER DUET LASER SYSTEM
K060338 FAMILY OF SELECTA LASER SYSTEMS INCLUDING SELECTA 1064, SELECTA SLT, SELECTA DUET, SELECTA DUO, SELECTA TRIO
Search all 43 clearances from Lumenis, Inc. →