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FDA 510(k)

MAX L SYSTEM

K-Number: K761168 · 1976-12-10

ApplicantBrinkman Instruments, Inc.
Decision Date1976-12-10
Product CodeDPM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAX L SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Brinkman Instruments, Inc.. It received FDA 510(k) clearance on 1976-12-10 under 510(k) number K761168. The device is classified under product code DPM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAX L SYSTEM?

MAX L SYSTEM is a medical device that received FDA 510(k) clearance on 1976-12-10. The listed applicant is Brinkman Instruments, Inc.. The 510(k) number is K761168.

When did MAX L SYSTEM receive FDA 510(k) clearance?

MAX L SYSTEM received FDA 510(k) clearance on 1976-12-10, under 510(k) number K761168.

Who is the listed applicant for MAX L SYSTEM?

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

What is the FDA product code for MAX L SYSTEM?

The FDA product code for MAX L SYSTEM is DPM.

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Related Devices (Code: DPM)

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.

K952501TOX PERFECT B TUBES AND REAGENTSChimera Research & Chemical, Inc.K895105HIGH PRESSURE INERT PLASTIC COLUMNS FOR CLIN. USEWaters Chemical ProductsK894141LIQUID CHROMATOGRAPHY COLUMNSSupelco, Inc.K891673ADVANCED PURIFICATION GLASS COLUMNWaters Chemical ProductsK884403LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBESupelco, Inc.K881868LIQUID CHROMATOGRAPHY COLUMNS HISEP COLUMN & GUARDSupelco, Inc.

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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