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FDA 510(k)

DYNATECH SPD 2000, NUMBER 002-910-0000

K-Number: K881195 · 1988-06-07

ApplicantDynatech Laboratories, Inc.
Decision Date1988-06-07
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DYNATECH SPD 2000, NUMBER 002-910-0000 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Laboratories, Inc.. It received FDA 510(k) clearance on 1988-06-07 under 510(k) number K881195. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATECH SPD 2000, NUMBER 002-910-0000?

DYNATECH SPD 2000, NUMBER 002-910-0000 is a medical device that received FDA 510(k) clearance on 1988-06-07. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K881195.

When did DYNATECH SPD 2000, NUMBER 002-910-0000 receive FDA 510(k) clearance?

DYNATECH SPD 2000, NUMBER 002-910-0000 received FDA 510(k) clearance on 1988-06-07, under 510(k) number K881195.

Who is the listed applicant for DYNATECH SPD 2000, NUMBER 002-910-0000?

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

What is the FDA product code for DYNATECH SPD 2000, NUMBER 002-910-0000?

The FDA product code for DYNATECH SPD 2000, NUMBER 002-910-0000 is JQW.

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Other records listing Dynatech Laboratories, Inc. as applicant

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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