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FDA 510(k)

PHOTOMETER LP 300

K-Number: K832531 · 1983-12-12

ApplicantDr. Bruno Lange GmbH
Decision Date1983-12-12
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHOTOMETER LP 300 is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Bruno Lange GmbH. It received FDA 510(k) clearance on 1983-12-12 under 510(k) number K832531. 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 PHOTOMETER LP 300?

PHOTOMETER LP 300 is a medical device that received FDA 510(k) clearance on 1983-12-12. The listed applicant is Dr. Bruno Lange GmbH. The 510(k) number is K832531.

When did PHOTOMETER LP 300 receive FDA 510(k) clearance?

PHOTOMETER LP 300 received FDA 510(k) clearance on 1983-12-12, under 510(k) number K832531.

Who is the listed applicant for PHOTOMETER LP 300?

The FDA 510(k) record lists Dr. Bruno Lange GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHOTOMETER LP 300?

The FDA product code for PHOTOMETER LP 300 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 Dr. Bruno Lange GmbH 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.

K834226FLAME PHOTOMETERSK801564PHOTOMETER LP 1K801562PHOTOMETER LP 6K801563PHOTOMETER LP 3

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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