FDA 510(k)

DYNATECH SPD 3000, #002-900-0000

K-Number: K872363 · 1987-07-16

Decision Date1987-07-16

Product CodeJQW

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

DYNATECH SPD 3000, #002-900-0000 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 1987-07-16 under 510(k) number K872363. 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 3000, #002-900-0000?

DYNATECH SPD 3000, #002-900-0000 is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K872363.

When did DYNATECH SPD 3000, #002-900-0000 receive FDA 510(k) clearance?

DYNATECH SPD 3000, #002-900-0000 received FDA 510(k) clearance on 1987-07-16, under 510(k) number K872363.

Who is the listed applicant for DYNATECH SPD 3000, #002-900-0000?

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 3000, #002-900-0000?

The FDA product code for DYNATECH SPD 3000, #002-900-0000 is JQW.

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Other records listing Dynatech Laboratories, Inc. as applicant

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Related Devices (Code: JQW)

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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.