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FDA 510(k)

MINI-SHAKER

K-Number: K813318 · 1981-12-17

ApplicantDynatech Corp.
Decision Date1981-12-17
Product CodeJRQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINI-SHAKER is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1981-12-17 under 510(k) number K813318. 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 MINI-SHAKER?

MINI-SHAKER is a medical device that received FDA 510(k) clearance on 1981-12-17. The listed applicant is Dynatech Corp.. The 510(k) number is K813318.

When did MINI-SHAKER receive FDA 510(k) clearance?

MINI-SHAKER received FDA 510(k) clearance on 1981-12-17, under 510(k) number K813318.

Who is the listed applicant for MINI-SHAKER?

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

What is the FDA product code for MINI-SHAKER?

The FDA product code for MINI-SHAKER is JRQ.

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Other records listing Dynatech Corp. 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.

K904567DYNATECH MR4000 MICROPLATE READERK854603MULTI MASH 2000K854602MINI MASH 2000K854604AUTO MASHK832117IMMULON SUBSTRATE REMOVAWELL STRIPSK823787HANDI-WASH

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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.

K813148S/P VORTEX MIXERAmerican DadeK813149S/P VORTEX MIXER JR.American DadeK801145SMI MULTI-TUBE VORTEXERScientific Manufacturing IndustriesK790753DIMENSIONALL ROTATORAmerican Hospital Supply Corp.K790027SHAKER, MODEL SH-510Sysmex Corp.K780543THERMAJUST CIRCU-TEMPTechhnilab Instruments, 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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