SYNCHRON SYSTEMS CAL 5 PLUS
K-Number: K971283 · 1997-06-03
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Device Summary
Frequently Asked Questions
What is the SYNCHRON SYSTEMS CAL 5 PLUS?
SYNCHRON SYSTEMS CAL 5 PLUS is a medical device that received FDA 510(k) clearance on 1997-06-03. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K971283.
When did SYNCHRON SYSTEMS CAL 5 PLUS receive FDA 510(k) clearance?
SYNCHRON SYSTEMS CAL 5 PLUS received FDA 510(k) clearance on 1997-06-03, under 510(k) number K971283.
Who is the listed applicant for SYNCHRON SYSTEMS CAL 5 PLUS?
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 SYNCHRON SYSTEMS CAL 5 PLUS?
The FDA product code for SYNCHRON SYSTEMS CAL 5 PLUS is JIX.
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: JIX)
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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