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FDA 510(k)

ELECTROLYTE ANALYZER ACCESSORY

K-Number: K820118 · 1982-02-04

ApplicantBoehringer Mannheim Corp.
Decision Date1982-02-04
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTROLYTE ANALYZER ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1982-02-04 under 510(k) number K820118. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROLYTE ANALYZER ACCESSORY?

ELECTROLYTE ANALYZER ACCESSORY is a medical device that received FDA 510(k) clearance on 1982-02-04. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K820118.

When did ELECTROLYTE ANALYZER ACCESSORY receive FDA 510(k) clearance?

ELECTROLYTE ANALYZER ACCESSORY received FDA 510(k) clearance on 1982-02-04, under 510(k) number K820118.

Who is the listed applicant for ELECTROLYTE ANALYZER ACCESSORY?

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

What is the FDA product code for ELECTROLYTE ANALYZER ACCESSORY?

The FDA product code for ELECTROLYTE ANALYZER ACCESSORY is JJE.

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Related Devices (Code: JJE)

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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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