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

LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER

K Number: K902056 · Decision Oct 30, 1990
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
7
Applicant Total
85
Review Days
176

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Basic Information

Device Name
LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER
K Number
K902056
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4220
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Hollister, Inc.
Date Received
May 7, 1990
Decision Date
October 30, 1990
Product Code
JDY
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
JDY Evacuator, Vapor, Cement Monomer

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Other Clearances by Hollister, Inc.

K Number Device Name
K123804 INSTAFLO BOWEL CATHETER SYSTEM KIT
K100273 INSTAFLO BOWEL CATHETER SYSTEM KIT
K090960 VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184,
K083153 ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007
K050483 EVADRI BLADDER CONTROL SYSTEMS
K040779 RESTORE WOUND CLEANSER
K013612 INCARE PELVIC FLOOR THERAPY SYSTEM
K013653 INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE
K013483 INCARE ADVANCE; INTERMITTENT CATHETER, PLUS INTERMITTENT CATHETER, PLUS KIT
K013345 INCARE INTERMITTENT CATHETER
Search all 85 clearances from Hollister, Inc. →