Medical Device Manufacturer · US , Indianapolis , IN

Perkinelmer, Inc. - FDA 510(k) Cleared Devices

17 submissions · 15 cleared · Since 2009

Total

Cleared

Denied

Perkinelmer, Inc. has 15 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Last cleared in 2022. Active since 2009. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Perkinelmer, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Perkinelmer, Inc.

17 devices

1-12 of 17

Cleared Nov 09, 2022

Eonis SCID-SMA kit

K203035 · PJI

Medical Genetics · 765d

Not Cleared Nov 09, 2022

Eonis SCID-SMA Kit

DEN200044 · QUE

Medical Genetics · 854d

Cleared Feb 07, 2020

NeoBase 2 Non-derivatized MSMS Kit

K193103 · NQL

Chemistry · 91d

Not Cleared Dec 12, 2019

GSP Neonatal Creatine Kinase - MM kit

DEN180056 · QJE

Chemistry · 427d

Cleared Nov 06, 2019

GSP Neonatal Total Galactose kit

PerkinElmer XRpad2 4336 HWC-M Flat Panel Detector

K161966 · MQB

Radiology · 52d

Cleared Sep 01, 2016

PerkinElmer, XRpad2 3025 HWC-M Flat Panel Detector

K161942 · MQB

Radiology · 48d

Cleared Oct 23, 2014

PerkinElmer, XRpad 4343 F MED Flat Panel Detector

K142698 · MQB

Radiology · 31d

Cleared Aug 01, 2014

PERKINELMER, XRPAD 4336 MED FLAT PANEL DETECTOR

K140551 · MQB

Radiology · 150d

Cleared Mar 12, 2013

PERKINELMER 226 SAMPLE COLLECTION DEVICES

K121864 · PJC

Chemistry · 259d

Cleared Nov 28, 2012

PERKINELMER XRD 1622 AP3 MED FLAT PANEL DETECTOR

K122495 · MQB

Radiology · 104d

Perkinelmer, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Perkinelmer, Inc.

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