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FDA 510(k)

VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM

K-Number: K851945 · 1985-05-24

ApplicantVarian Assoc., Inc.
Decision Date1985-05-24
Product CodeKZR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM 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 1985-05-24 under 510(k) number K851945. The device is classified under product code KZR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM?

VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM is a medical device that received FDA 510(k) clearance on 1985-05-24. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K851945.

When did VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM receive FDA 510(k) clearance?

VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM received FDA 510(k) clearance on 1985-05-24, under 510(k) number K851945.

Who is the listed applicant for VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM?

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

What is the FDA product code for VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM?

The FDA product code for VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM is KZR.

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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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Related Devices (Code: KZR)

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.

K9730742487 DUAL WAVELENGTH ABSORBANCE DETECTORWaters CorporationK931227USDT FLOW IMMUNOASSAY SYSTEM, MODEL 9000U.S. Drug Testing, Inc.K905538COLUMNS LIQUID CHROMATOGRAPHY DPMMillpore Corp.K861392SYVA SOLID PHASE COLUMNS SYSTEM IISyva Co.K860197SERIES 410 LC PUMPThe Perkin-Elmer Corp.K843568LIQUID CHROMATOGRAPH 400The Perkin-Elmer Corp.

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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