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FDA 510(k)

ATOMIC ABSORPTION SPECTROPHOTOMETER,

K-Number: K790780 · 1979-05-03

Decision Date1979-05-03
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ATOMIC ABSORPTION SPECTROPHOTOMETER, 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 K790780. 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 ATOMIC ABSORPTION SPECTROPHOTOMETER,?

ATOMIC ABSORPTION SPECTROPHOTOMETER, 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 K790780.

When did ATOMIC ABSORPTION SPECTROPHOTOMETER, receive FDA 510(k) clearance?

ATOMIC ABSORPTION SPECTROPHOTOMETER, received FDA 510(k) clearance on 1979-05-03, under 510(k) number K790780.

Who is the listed applicant for ATOMIC ABSORPTION SPECTROPHOTOMETER,?

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 ATOMIC ABSORPTION SPECTROPHOTOMETER,?

The FDA product code for ATOMIC ABSORPTION SPECTROPHOTOMETER, 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.

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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