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FDA 510(k)

BERTHOLD LB 954

K-Number: K922329 · 1992-11-16

ApplicantEg&G Berthold Analytical Instruments, Inc.
Decision Date1992-11-16
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BERTHOLD LB 954 is the device name listed in this FDA 510(k) record. The listed applicant is Eg&G Berthold Analytical Instruments, Inc.. It received FDA 510(k) clearance on 1992-11-16 under 510(k) number K922329. 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 BERTHOLD LB 954?

BERTHOLD LB 954 is a medical device that received FDA 510(k) clearance on 1992-11-16. The listed applicant is Eg&G Berthold Analytical Instruments, Inc.. The 510(k) number is K922329.

When did BERTHOLD LB 954 receive FDA 510(k) clearance?

BERTHOLD LB 954 received FDA 510(k) clearance on 1992-11-16, under 510(k) number K922329.

Who is the listed applicant for BERTHOLD LB 954?

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

What is the FDA product code for BERTHOLD LB 954?

The FDA product code for BERTHOLD LB 954 is JJQ.

Related Clinical Trials

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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Other records listing Eg&G 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.

K922976LB 9502- CLINILUMAT, LB 953 - AUTO-CLIMILUMAT

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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.

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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