Perkinelmer Life Sciences, Inc.

FDA Regulatory Profile

Perkinelmer Life Sciences, Inc. appears in FDA public data with 2 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0728-2018, Class III) was initiated on August 2, 2017. Its most recent 510(k) clearance was granted on August 24, 2004.

Summary

Total Recalls
2
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0728-2018Class IIIJANUS & JANUS G3 Automated Workstation is an automated programmable liquid handling instrument inteAugust 2, 2017
Z-2685-2017Class IIMultiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part NuMay 15, 2017

Recent 510(k) Clearances

K-NumberDeviceDate
DEN040002NEOGRAM AMINO ACIDS AND ACYLCARNITINES TANDEM MASS SPECTROMETRY KIT, MODEL MS-8970August 24, 2004
K021541NEOGRAM PKU TANDEM MASS SPECTROMETRY KITOctober 28, 2002