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FDA 510(k)

LITHIUM INTERNAL STANDARD 1 MEQ/L #60085

K-Number: K871185 · 1987-05-28

ApplicantIn Vitro Diagnostics, Inc.
Decision Date1987-05-28
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LITHIUM INTERNAL STANDARD 1 MEQ/L #60085 is the device name listed in this FDA 510(k) record. The listed applicant is In Vitro Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-05-28 under 510(k) number K871185. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITHIUM INTERNAL STANDARD 1 MEQ/L #60085?

LITHIUM INTERNAL STANDARD 1 MEQ/L #60085 is a medical device that received FDA 510(k) clearance on 1987-05-28. The listed applicant is In Vitro Diagnostics, Inc.. The 510(k) number is K871185.

When did LITHIUM INTERNAL STANDARD 1 MEQ/L #60085 receive FDA 510(k) clearance?

LITHIUM INTERNAL STANDARD 1 MEQ/L #60085 received FDA 510(k) clearance on 1987-05-28, under 510(k) number K871185.

Who is the listed applicant for LITHIUM INTERNAL STANDARD 1 MEQ/L #60085?

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

What is the FDA product code for LITHIUM INTERNAL STANDARD 1 MEQ/L #60085?

The FDA product code for LITHIUM INTERNAL STANDARD 1 MEQ/L #60085 is JIS.

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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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