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FDA 510(k)

BDS-3 BEAM DATA SCANNER

K-Number: K844620 · 1985-07-01

ApplicantVarian Assoc., Inc.
Decision Date1985-07-01
Product CodeLHO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BDS-3 BEAM DATA SCANNER 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 1985-07-01 under 510(k) number K844620. The device is classified under product code LHO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BDS-3 BEAM DATA SCANNER?

BDS-3 BEAM DATA SCANNER is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K844620.

When did BDS-3 BEAM DATA SCANNER receive FDA 510(k) clearance?

BDS-3 BEAM DATA SCANNER received FDA 510(k) clearance on 1985-07-01, under 510(k) number K844620.

Who is the listed applicant for BDS-3 BEAM DATA SCANNER?

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 BDS-3 BEAM DATA SCANNER?

The FDA product code for BDS-3 BEAM DATA SCANNER is LHO.

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Other records listing Varian Assoc., Inc. as applicant

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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.

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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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