FDA 510(k)

MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL

K-Number: K881503 · 1988-07-08

Decision Date1988-07-08

Product CodeJJY

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1988-07-08 under 510(k) number K881503. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL?

MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL is a medical device that received FDA 510(k) clearance on 1988-07-08. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K881503.

When did MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL receive FDA 510(k) clearance?

MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL received FDA 510(k) clearance on 1988-07-08, under 510(k) number K881503.

Who is the listed applicant for MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL?

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

What is the FDA product code for MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL?

The FDA product code for MODIFIED DADE COMPRE. ELECTROPHORESIS CONTROL is JJY.

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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.