PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO
K-Number: K884864 · 1989-02-10
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Device Summary
Frequently Asked Questions
What is the PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO?
PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO is a medical device that received FDA 510(k) clearance on 1989-02-10. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K884864.
When did PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO receive FDA 510(k) clearance?
PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO received FDA 510(k) clearance on 1989-02-10, under 510(k) number K884864.
Who is the listed applicant for PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION 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 PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO?
The FDA product code for PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTRO is JJQ.
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.
Related Devices (Code: JJQ)
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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