FDA 510(k)

LKB-WALLACE 1251 LUMINOMETER

K-Number: K820217 · 1982-02-12

Decision Date1982-02-12

Product CodeJJQ

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

LKB-WALLACE 1251 LUMINOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Lkb Instruments, Inc.. It received FDA 510(k) clearance on 1982-02-12 under 510(k) number K820217. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LKB-WALLACE 1251 LUMINOMETER?

LKB-WALLACE 1251 LUMINOMETER is a medical device that received FDA 510(k) clearance on 1982-02-12. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K820217.

When did LKB-WALLACE 1251 LUMINOMETER receive FDA 510(k) clearance?

LKB-WALLACE 1251 LUMINOMETER received FDA 510(k) clearance on 1982-02-12, under 510(k) number K820217.

Who is the listed applicant for LKB-WALLACE 1251 LUMINOMETER?

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

What is the FDA product code for LKB-WALLACE 1251 LUMINOMETER?

The FDA product code for LKB-WALLACE 1251 LUMINOMETER is JJQ.

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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.