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FDA 510(k)

CHROMATOGRAPHY ANALYSIS SYS, MODEL 8500

K-Number: K770827 · 1977-07-21

ApplicantVarian Assoc., Inc.
Decision Date1977-07-21
Product Code
DecisionSubstantially Equivalent

Device Summary

CHROMATOGRAPHY ANALYSIS SYS, MODEL 8500 is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1977-07-21 under 510(k) number K770827. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHROMATOGRAPHY ANALYSIS SYS, MODEL 8500?

CHROMATOGRAPHY ANALYSIS SYS, MODEL 8500 is a medical device that received FDA 510(k) clearance on 1977-07-21. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K770827.

When did CHROMATOGRAPHY ANALYSIS SYS, MODEL 8500 receive FDA 510(k) clearance?

CHROMATOGRAPHY ANALYSIS SYS, MODEL 8500 received FDA 510(k) clearance on 1977-07-21, under 510(k) number K770827.

Who is the listed applicant for CHROMATOGRAPHY ANALYSIS SYS, MODEL 8500?

The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Varian Assoc., Inc. 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.

K000922PROTON VISIONK992762BRACHYVISION 6.0K992751SOMAVISIONK992753CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEMK990085MILLENNIUM MLC -120K980601VARISOURCE WRIGHT VAGINAL CUFF APPLICATOR FOR VARIAN VARISOURCE REMOTE HIGH DOSE RATE AFTERIOADER

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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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