Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SPECTROPHOTOMETER SYSTEM, MODEL AA-475

K-Number: K790781 · 1979-05-03

ApplicantVarian Assoc., Inc.
Decision Date1979-05-03
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETER SYSTEM, MODEL AA-475 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 1979-05-03 under 510(k) number K790781. The device is classified under product code JXR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTROPHOTOMETER SYSTEM, MODEL AA-475?

SPECTROPHOTOMETER SYSTEM, MODEL AA-475 is a medical device that received FDA 510(k) clearance on 1979-05-03. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K790781.

When did SPECTROPHOTOMETER SYSTEM, MODEL AA-475 receive FDA 510(k) clearance?

SPECTROPHOTOMETER SYSTEM, MODEL AA-475 received FDA 510(k) clearance on 1979-05-03, under 510(k) number K790781.

Who is the listed applicant for SPECTROPHOTOMETER SYSTEM, MODEL AA-475?

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 SPECTROPHOTOMETER SYSTEM, MODEL AA-475?

The FDA product code for SPECTROPHOTOMETER SYSTEM, MODEL AA-475 is JXR.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 86 devices →

Related Devices (Code: JXR)

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.

K900828PERKIN-ELMER AA 3100 ATOMIC ABSORPTION SPECTRO.The Perkin-Elmer Corp.K875098CIBA CORNING MODEL 644Ciba Corning Diagnostics Corp.K842752ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOTThe Perkin-Elmer Corp.K842496ICP/6500 INDUCTIVELY-COUPLED PLASMA-The Perkin-Elmer Corp.K830799INDUCTIVELY-COUPLED PLASMA SPECTROMETERThe Perkin-Elmer Corp.K820320MODEL 3030 ATOMIC ABSORPTION SPECTRO-The 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.

↑