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Perlink USA, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K922358STERLING POWDER FREE PATIENT EXAMINATION GLOVESJune 11, 1993
K924959STERLING LATEX EXAM GLOVE, HYPO-ALLERGENICMarch 3, 1993
K921438DISPOSABLE LATEX EXAMINATION GLOVESJune 23, 1992
K896707PERLINK SCREEN, KIRAN SCREENAugust 30, 1990
K901790THERMOMETER, MERCURY/CLINICALJuly 11, 1990
K896708PERLINK CASSETTE, KIRAN CASSETTEMay 7, 1990