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FDA 510(k)

PHOTOMETER LP 6

K-Number: K801562 · 1980-08-20

ApplicantDr. Bruno Lange GmbH
Decision Date1980-08-20
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHOTOMETER LP 6 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 1980-08-20 under 510(k) number K801562. 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 6?

PHOTOMETER LP 6 is a medical device that received FDA 510(k) clearance on 1980-08-20. The listed applicant is Dr. Bruno Lange GmbH. The 510(k) number is K801562.

When did PHOTOMETER LP 6 receive FDA 510(k) clearance?

PHOTOMETER LP 6 received FDA 510(k) clearance on 1980-08-20, under 510(k) number K801562.

Who is the listed applicant for PHOTOMETER LP 6?

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 6?

The FDA product code for PHOTOMETER LP 6 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 PHOTOMETERSK832531PHOTOMETER LP 300K801564PHOTOMETER LP 1K801563PHOTOMETER 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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