SERIES II LIQUID CHROMATOGRAPH
K-Number: K761219 · 1977-02-01
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Device Summary
Frequently Asked Questions
What is the SERIES II LIQUID CHROMATOGRAPH?
SERIES II LIQUID CHROMATOGRAPH is a medical device that received FDA 510(k) clearance on 1977-02-01. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K761219.
When did SERIES II LIQUID CHROMATOGRAPH receive FDA 510(k) clearance?
SERIES II LIQUID CHROMATOGRAPH received FDA 510(k) clearance on 1977-02-01, under 510(k) number K761219.
Who is the listed applicant for SERIES II LIQUID CHROMATOGRAPH?
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 SERIES II LIQUID CHROMATOGRAPH?
The FDA product code for SERIES II LIQUID CHROMATOGRAPH is KIE.
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: KIE)
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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