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FDA 510(k)

LKB 2164 MACRO-SPIN R CENTRIFUGE

K-Number: K831942 · 1983-07-29

ApplicantLkb Instruments, Inc.
Decision Date1983-07-29
Product CodeJQC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LKB 2164 MACRO-SPIN R CENTRIFUGE 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 1983-07-29 under 510(k) number K831942. The device is classified under product code JQC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LKB 2164 MACRO-SPIN R CENTRIFUGE?

LKB 2164 MACRO-SPIN R CENTRIFUGE is a medical device that received FDA 510(k) clearance on 1983-07-29. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K831942.

When did LKB 2164 MACRO-SPIN R CENTRIFUGE receive FDA 510(k) clearance?

LKB 2164 MACRO-SPIN R CENTRIFUGE received FDA 510(k) clearance on 1983-07-29, under 510(k) number K831942.

Who is the listed applicant for LKB 2164 MACRO-SPIN R CENTRIFUGE?

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 2164 MACRO-SPIN R CENTRIFUGE?

The FDA product code for LKB 2164 MACRO-SPIN R CENTRIFUGE is JQC.

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Other records listing Lkb Instruments, Inc. as applicant

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Related Devices (Code: JQC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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