FDA 510(k)

LITHIUM STANDARD (1MM/L)

K-Number: K800042 · 1980-01-21

Decision Date1980-01-21

Product CodeJIS

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

LITHIUM STANDARD (1MM/L) is the device name listed in this FDA 510(k) record. The listed applicant is Gilford Diagnostics. It received FDA 510(k) clearance on 1980-01-21 under 510(k) number K800042. 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 STANDARD (1MM/L)?

LITHIUM STANDARD (1MM/L) is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Gilford Diagnostics. The 510(k) number is K800042.

When did LITHIUM STANDARD (1MM/L) receive FDA 510(k) clearance?

LITHIUM STANDARD (1MM/L) received FDA 510(k) clearance on 1980-01-21, under 510(k) number K800042.

Who is the listed applicant for LITHIUM STANDARD (1MM/L)?

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

What is the FDA product code for LITHIUM STANDARD (1MM/L)?

The FDA product code for LITHIUM STANDARD (1MM/L) 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.