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FDA 510(k)

AUTODILUTER III

K-Number: K810659 · 1981-03-31

ApplicantDynatech Corp.
Decision Date1981-03-31
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AUTODILUTER III is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1981-03-31 under 510(k) number K810659. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTODILUTER III?

AUTODILUTER III is a medical device that received FDA 510(k) clearance on 1981-03-31. The listed applicant is Dynatech Corp.. The 510(k) number is K810659.

When did AUTODILUTER III receive FDA 510(k) clearance?

AUTODILUTER III received FDA 510(k) clearance on 1981-03-31, under 510(k) number K810659.

Who is the listed applicant for AUTODILUTER III?

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 AUTODILUTER III?

The FDA product code for AUTODILUTER III is JTC.

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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: JTC)

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.

K924907FILTERMATE UNIVERSAL HARVESTERPackard Instrument Co., Inc.K901808MICROMATE 196 MODEL A961960Packard Instrument Co., Inc.K894645IMMULON 1,2,3,AND 4 DIVIDASTRIPS TMDynatech Laboratories, Inc.K892369MULTI-PROBE HEAD PLUSHamilton Co.K891766GENETIC SYSTEMS MICROPLATE STRIP WASHERGenetic Systems Corp.K891765GENETIC SYSTEMS PIPETTOR/DILUTORGenetic Systems Corp.

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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