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FDA 510(k)

ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT

K-Number: K842752 · 1984-08-22

Decision Date1984-08-22
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT 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 1984-08-22 under 510(k) number K842752. 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 ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT?

ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT is a medical device that received FDA 510(k) clearance on 1984-08-22. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K842752.

When did ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT receive FDA 510(k) clearance?

ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT received FDA 510(k) clearance on 1984-08-22, under 510(k) number K842752.

Who is the listed applicant for ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT?

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 ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT?

The FDA product code for ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT 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

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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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