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FDA 510(k)

MODULAR MASS SPECTROMETER (M.S.)

K-Number: K862605 · 1986-08-13

ApplicantThe Perkin-Elmer Corp.
Decision Date1986-08-13
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODULAR MASS SPECTROMETER (M.S.) is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1986-08-13 under 510(k) number K862605. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR MASS SPECTROMETER (M.S.)?

MODULAR MASS SPECTROMETER (M.S.) is a medical device that received FDA 510(k) clearance on 1986-08-13. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K862605.

When did MODULAR MASS SPECTROMETER (M.S.) receive FDA 510(k) clearance?

MODULAR MASS SPECTROMETER (M.S.) received FDA 510(k) clearance on 1986-08-13, under 510(k) number K862605.

Who is the listed applicant for MODULAR MASS SPECTROMETER (M.S.)?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODULAR MASS SPECTROMETER (M.S.)?

The FDA product code for MODULAR MASS SPECTROMETER (M.S.) is CCK.

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Other records listing The Perkin-Elmer Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPK900828PERKIN-ELMER AA 3100 ATOMIC ABSORPTION SPECTRO.K884864PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTROK884886MODEL 250 LIQUID CHROMOTAGRAPHY PUMPK872737PERKIN-ELMER LC235 DIODE ARRAY DETECTORK872464ION TRAP DETECTOR (ITD)

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Related Devices (Code: CCK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251641GF-310R Multigas Unit (GF-310R)Nihon Kohden CorporationK261633VisuBreathAffirm Medical Technologies II, LLCK253030Capnostream™35 Portable Respiratory Monitor (PM35MN)Covidien, LLCK250148Medical Gas Analyzer (AG200)Prior Care Science Technology, Ltd.K243956TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)Nihon Kohden CorporationK2512160184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling lineBarbaras Development, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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