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FDA 510(k)

KD 0.02 M CALCIUM CHLORIDE SOLUTION

K-Number: K883637 · 1988-10-31

ApplicantKing Diagnostics, Inc.
Decision Date1988-10-31
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

KD 0.02 M CALCIUM CHLORIDE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is King Diagnostics, Inc.. It received FDA 510(k) clearance on 1988-10-31 under 510(k) number K883637. 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 KD 0.02 M CALCIUM CHLORIDE SOLUTION?

KD 0.02 M CALCIUM CHLORIDE SOLUTION is a medical device that received FDA 510(k) clearance on 1988-10-31. The listed applicant is King Diagnostics, Inc.. The 510(k) number is K883637.

When did KD 0.02 M CALCIUM CHLORIDE SOLUTION receive FDA 510(k) clearance?

KD 0.02 M CALCIUM CHLORIDE SOLUTION received FDA 510(k) clearance on 1988-10-31, under 510(k) number K883637.

Who is the listed applicant for KD 0.02 M CALCIUM CHLORIDE SOLUTION?

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

What is the FDA product code for KD 0.02 M CALCIUM CHLORIDE SOLUTION?

The FDA product code for KD 0.02 M CALCIUM CHLORIDE 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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