LIQUID SCINTILLATION SPECTROPHOTOMETER
K-Number: K810345 · 1981-02-25
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Device Summary
Frequently Asked Questions
What is the LIQUID SCINTILLATION SPECTROPHOTOMETER?
LIQUID SCINTILLATION SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K810345.
When did LIQUID SCINTILLATION SPECTROPHOTOMETER receive FDA 510(k) clearance?
LIQUID SCINTILLATION SPECTROPHOTOMETER received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810345.
Who is the listed applicant for LIQUID SCINTILLATION SPECTROPHOTOMETER?
The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUID SCINTILLATION SPECTROPHOTOMETER?
The FDA product code for LIQUID SCINTILLATION SPECTROPHOTOMETER is JJJ.
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 Beckman Instruments, Inc. 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: JJJ)
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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