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FDA 510(k)

LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT

K-Number: K872324 · 1987-08-19

ApplicantBerthold Analytical Instruments, Inc.
Decision Date1987-08-19
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT is the device name listed in this FDA 510(k) record. The listed applicant is Berthold Analytical Instruments, Inc.. It received FDA 510(k) clearance on 1987-08-19 under 510(k) number K872324. 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 LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT?

LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT is a medical device that received FDA 510(k) clearance on 1987-08-19. The listed applicant is Berthold Analytical Instruments, Inc.. The 510(k) number is K872324.

When did LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT receive FDA 510(k) clearance?

LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT received FDA 510(k) clearance on 1987-08-19, under 510(k) number K872324.

Who is the listed applicant for LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT?

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

What is the FDA product code for LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT?

The FDA product code for LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT is JJQ.

Related Clinical Trials

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Other records listing Berthold Analytical Instruments, Inc. as applicant

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.

K870115BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS

Related Devices (Code: JJQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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