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FDA 510(k)

CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION

K-Number: K924509 · 1992-12-21

ApplicantBehring Diagnostics, Inc.
Decision Date1992-12-21
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1992-12-21 under 510(k) number K924509. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION?

CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION is a medical device that received FDA 510(k) clearance on 1992-12-21. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K924509.

When did CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION receive FDA 510(k) clearance?

CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION received FDA 510(k) clearance on 1992-12-21, under 510(k) number K924509.

Who is the listed applicant for CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION?

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

What is the FDA product code for CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION?

The FDA product code for CALCIUM CHLORIDE/DIETHYLBARB ACETATE BUFF SOLUTION is JPA.

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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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