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FDA 510(k)

MODEL 3030 ATOMIC ABSORPTION SPECTRO-

K-Number: K820320 · 1982-03-01

Decision Date1982-03-01
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL 3030 ATOMIC ABSORPTION SPECTRO- is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1982-03-01 under 510(k) number K820320. 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 MODEL 3030 ATOMIC ABSORPTION SPECTRO-?

MODEL 3030 ATOMIC ABSORPTION SPECTRO- is a medical device that received FDA 510(k) clearance on 1982-03-01. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K820320.

When did MODEL 3030 ATOMIC ABSORPTION SPECTRO- receive FDA 510(k) clearance?

MODEL 3030 ATOMIC ABSORPTION SPECTRO- received FDA 510(k) clearance on 1982-03-01, under 510(k) number K820320.

Who is the listed applicant for MODEL 3030 ATOMIC ABSORPTION SPECTRO-?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 3030 ATOMIC ABSORPTION SPECTRO-?

The FDA product code for MODEL 3030 ATOMIC ABSORPTION SPECTRO- 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 The Perkin-Elmer Corp. 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 62 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

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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