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

LARYNGOSCOPE COVER

K Number: K945301 · Decision May 31, 1996
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
63
Applicant Total
1
Review Days
578

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
LARYNGOSCOPE COVER
K Number
K945301
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5540
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sotiria Mourkidou, M.D.
Date Received
October 31, 1994
Decision Date
May 31, 1996
Product Code
CCW
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CCW Laryngoscope, Rigid

Similar 510(k) Clearances

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

View all