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FDA 510(k)

FLOW-CALIBRATION MODULE

K-Number: K831758 · 1983-07-19

ApplicantThe Perkin-Elmer Corp.
Decision Date1983-07-19
Product CodeBXW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOW-CALIBRATION MODULE 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 1983-07-19 under 510(k) number K831758. The device is classified under product code BXW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW-CALIBRATION MODULE?

FLOW-CALIBRATION MODULE is a medical device that received FDA 510(k) clearance on 1983-07-19. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K831758.

When did FLOW-CALIBRATION MODULE receive FDA 510(k) clearance?

FLOW-CALIBRATION MODULE received FDA 510(k) clearance on 1983-07-19, under 510(k) number K831758.

Who is the listed applicant for FLOW-CALIBRATION MODULE?

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 FLOW-CALIBRATION MODULE?

The FDA product code for FLOW-CALIBRATION MODULE is BXW.

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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: BXW)

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.

K853848RESPIRATORY DIAGNOSTIC EQUIPMENT CALIBRATORMedical Graphics Corp.K830898SYRINGE 500BC BE #7000Instrumentation Industries, Inc.K812765DATASCRIBE #DS-40Timeter Instrument Corp.K810290OHIO CAL-CHEKOhio Medical ProductsK760520CALIPERS, MCGAW SKINFOLDMcgaw Laboratories

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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