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FDA 510(k)

DIMENSION AHDL CALIBRATOR

K-Number: K983850 · 1998-11-18

ApplicantDade Behring, Inc.
Decision Date1998-11-18
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIMENSION AHDL CALIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dade Behring, Inc.. It received FDA 510(k) clearance on 1998-11-18 under 510(k) number K983850. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIMENSION AHDL CALIBRATOR?

DIMENSION AHDL CALIBRATOR is a medical device that received FDA 510(k) clearance on 1998-11-18. The listed applicant is Dade Behring, Inc.. The 510(k) number is K983850.

When did DIMENSION AHDL CALIBRATOR receive FDA 510(k) clearance?

DIMENSION AHDL CALIBRATOR received FDA 510(k) clearance on 1998-11-18, under 510(k) number K983850.

Who is the listed applicant for DIMENSION AHDL CALIBRATOR?

The FDA 510(k) record lists Dade Behring, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIMENSION AHDL CALIBRATOR?

The FDA product code for DIMENSION AHDL CALIBRATOR is JIT.

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Other records listing Dade Behring, Inc. as applicant

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Related Devices (Code: JIT)

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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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