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FDA 510(k)

MMB CALIBRATOR

K-Number: K970336 · 1997-03-03

ApplicantDade Chemistry Systems, Inc.
Decision Date1997-03-03
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MMB CALIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dade Chemistry Systems, Inc.. It received FDA 510(k) clearance on 1997-03-03 under 510(k) number K970336. 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 MMB CALIBRATOR?

MMB CALIBRATOR is a medical device that received FDA 510(k) clearance on 1997-03-03. The listed applicant is Dade Chemistry Systems, Inc.. The 510(k) number is K970336.

When did MMB CALIBRATOR receive FDA 510(k) clearance?

MMB CALIBRATOR received FDA 510(k) clearance on 1997-03-03, under 510(k) number K970336.

Who is the listed applicant for MMB CALIBRATOR?

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

What is the FDA product code for MMB CALIBRATOR?

The FDA product code for MMB CALIBRATOR is JIT.

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Other records listing Dade Chemistry Systems, Inc. as applicant

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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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