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FDA 510(k)

MICRO LOWRY PROTEINTEST

K-Number: K792347 · 1979-12-06

ApplicantPanmed, Inc.
Decision Date1979-12-06
Product CodeJGP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICRO LOWRY PROTEINTEST is the device name listed in this FDA 510(k) record. The listed applicant is Panmed, Inc.. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792347. The device is classified under product code JGP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO LOWRY PROTEINTEST?

MICRO LOWRY PROTEINTEST is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Panmed, Inc.. The 510(k) number is K792347.

When did MICRO LOWRY PROTEINTEST receive FDA 510(k) clearance?

MICRO LOWRY PROTEINTEST received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792347.

Who is the listed applicant for MICRO LOWRY PROTEINTEST?

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

What is the FDA product code for MICRO LOWRY PROTEINTEST?

The FDA product code for MICRO LOWRY PROTEINTEST is JGP.

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Other records listing Panmed, Inc. as applicant

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Related Devices (Code: JGP)

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.

K070757MICROPROTEIN REAGENT SETPointe Scientific, Inc.,K964960VITROS CHEMISTRY PRODUCTS UPRO SLIDESJohnson & Johnson Clinical Diagnostics, Inc.K863112PROTEINMETERJ. D. Assoc.K821534HEMATOLOGY DATA MANAGEMENT SYSBiovation, 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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