FDA 510(k)

ABBOTT CATION SUPPLEMENT SOLUTION

K-Number: K853546 · 1985-09-06

Decision Date1985-09-06

Product CodeJSK

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

ABBOTT CATION SUPPLEMENT SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1985-09-06 under 510(k) number K853546. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABBOTT CATION SUPPLEMENT SOLUTION?

ABBOTT CATION SUPPLEMENT SOLUTION is a medical device that received FDA 510(k) clearance on 1985-09-06. The listed applicant is Abbott Laboratories. The 510(k) number is K853546.

When did ABBOTT CATION SUPPLEMENT SOLUTION receive FDA 510(k) clearance?

ABBOTT CATION SUPPLEMENT SOLUTION received FDA 510(k) clearance on 1985-09-06, under 510(k) number K853546.

Who is the listed applicant for ABBOTT CATION SUPPLEMENT SOLUTION?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABBOTT CATION SUPPLEMENT SOLUTION?

The FDA product code for ABBOTT CATION SUPPLEMENT SOLUTION is JSK.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.