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FDA 510(k)

MICRO-MIX PIPETTE SHAKER

K-Number: K770165 · 1977-01-31

ApplicantMaddak, Inc.
Decision Date1977-01-31
Product CodeJRQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICRO-MIX PIPETTE SHAKER is the device name listed in this FDA 510(k) record. The listed applicant is Maddak, Inc.. It received FDA 510(k) clearance on 1977-01-31 under 510(k) number K770165. The device is classified under product code JRQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-MIX PIPETTE SHAKER?

MICRO-MIX PIPETTE SHAKER is a medical device that received FDA 510(k) clearance on 1977-01-31. The listed applicant is Maddak, Inc.. The 510(k) number is K770165.

When did MICRO-MIX PIPETTE SHAKER receive FDA 510(k) clearance?

MICRO-MIX PIPETTE SHAKER received FDA 510(k) clearance on 1977-01-31, under 510(k) number K770165.

Who is the listed applicant for MICRO-MIX PIPETTE SHAKER?

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

What is the FDA product code for MICRO-MIX PIPETTE SHAKER?

The FDA product code for MICRO-MIX PIPETTE SHAKER is JRQ.

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.

Other records listing Maddak, 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.

View all 51 devices →

Related Devices (Code: JRQ)

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.

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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