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Effner and Spreine Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K875260
EFFNER CAUTERY INSTRUMENTS
June 6, 1988
K874755
EFFNER FE-EX* OROGASTRIC
April 6, 1988
K872480
KAHN-TACT U.S.A., EFF LARYNGOSCOPE
August 10, 1987
K852014
EFFNER SIMS RECTAL SPECULUM W/FIBER OPTIC ILLUMINA
August 7, 1985