PERKIN-ELMER LC235 DIODE ARRAY DETECTOR
K-Number: K872737 · 1987-09-18
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Device Summary
Frequently Asked Questions
What is the PERKIN-ELMER LC235 DIODE ARRAY DETECTOR?
PERKIN-ELMER LC235 DIODE ARRAY DETECTOR is a medical device that received FDA 510(k) clearance on 1987-09-18. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K872737.
When did PERKIN-ELMER LC235 DIODE ARRAY DETECTOR receive FDA 510(k) clearance?
PERKIN-ELMER LC235 DIODE ARRAY DETECTOR received FDA 510(k) clearance on 1987-09-18, under 510(k) number K872737.
Who is the listed applicant for PERKIN-ELMER LC235 DIODE ARRAY DETECTOR?
The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.
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.
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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