Mercury/Hydride Atomic Absorption Access

FDA 510(k) K781010 · The Perkin-Elmer Corp.

Substantially Equivalent

510(k) numberK781010

Submission

Device name
Mercury/Hydride Atomic Absorption Access
Applicant
The Perkin-Elmer Corp.
Mchenry, IL, US
Received
June 16, 1978
Decision date
July 27, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DPH – Mercury, Atomic Absorption
Device class
Class I (low risk)
Regulation
21 CFR 862.3600
Specialty
Clinical Toxicology

Other 510(k)s with product code DPH

510(k)DeviceApplicantDecision
K832933Gold Film Mercury Analyzer #511DPH · Traditional Jerome Instrument Corp.11/25/1983SE

More from Jerome Instrument Corp.

510(k)DeviceDecision
K935666Perkin-Elmer Series 200 Liq Chromatographic PumpKIE · Traditional 04/26/1994SE
K900828Perkin-Elmer Aa 3100 Atomic Absorption Spectro.JXR · Traditional 04/09/1990SE
K884864Plasma 40 Induct. Coupled Plasma Emmission SpectroJJQ · Traditional 02/10/1989SE
K884886Model 250 Liquid Chromotagraphy PumpLDM · Traditional 02/02/1989SE
K872737Perkin-Elmer LC235 Diode Array Detector · Traditional 09/18/1987SE
K872464Ion Trap Detector (Itd)DOP · Traditional 08/11/1987SE
K871550PFI-20 Polarizing FluorimeterKHO · Traditional 07/01/1987SE
K8721228000 Series Gas ChromatographsKZQ · Traditional 06/17/1987SE
K870661Lifewatch PlusBZQ · Traditional 03/09/1987SE
K862605Modular Mass Spectrometer (M.S.)CCK · Traditional 08/13/1986SE

Questions and answers

When was Mercury/Hydride Atomic Absorption Access cleared by the FDA?

Mercury/Hydride Atomic Absorption Access (K781010) received a 510(k) decision of Substantially Equivalent on July 27, 1978, 41 days after the submission was received.

What is the product code of K781010?

The FDA product code is DPH – Mercury, Atomic Absorption, a Class I (low risk) device regulated under 21 CFR 862.3600.