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)

MODEL MHS-20, ATOMIC ABSORPTION ACCESS

K-Number: K791074 · 1979-08-22

Decision Date1979-08-22
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL MHS-20, ATOMIC ABSORPTION ACCESS 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 1979-08-22 under 510(k) number K791074. 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 MHS-20, ATOMIC ABSORPTION ACCESS?

MODEL MHS-20, ATOMIC ABSORPTION ACCESS is a medical device that received FDA 510(k) clearance on 1979-08-22. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K791074.

When did MODEL MHS-20, ATOMIC ABSORPTION ACCESS receive FDA 510(k) clearance?

MODEL MHS-20, ATOMIC ABSORPTION ACCESS received FDA 510(k) clearance on 1979-08-22, under 510(k) number K791074.

Who is the listed applicant for MODEL MHS-20, ATOMIC ABSORPTION ACCESS?

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 MHS-20, ATOMIC ABSORPTION ACCESS?

The FDA product code for MODEL MHS-20, ATOMIC ABSORPTION ACCESS 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.

↑