BECKMAN CALIBRATOR 2 (CAL2)
K-Number: K973932 · 1997-12-15
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Device Summary
Frequently Asked Questions
What is the BECKMAN CALIBRATOR 2 (CAL2)?
BECKMAN CALIBRATOR 2 (CAL2) is a medical device that received FDA 510(k) clearance on 1997-12-15. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K973932.
When did BECKMAN CALIBRATOR 2 (CAL2) receive FDA 510(k) clearance?
BECKMAN CALIBRATOR 2 (CAL2) received FDA 510(k) clearance on 1997-12-15, under 510(k) number K973932.
Who is the listed applicant for BECKMAN CALIBRATOR 2 (CAL2)?
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 BECKMAN CALIBRATOR 2 (CAL2)?
The FDA product code for BECKMAN CALIBRATOR 2 (CAL2) 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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