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FDA 510(k)

SRD-2

K-Number: K781646 · 1978-10-27

ApplicantDynatech Laboratories, Inc.
Decision Date1978-10-27
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SRD-2 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 1978-10-27 under 510(k) number K781646. 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 SRD-2?

SRD-2 is a medical device that received FDA 510(k) clearance on 1978-10-27. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K781646.

When did SRD-2 receive FDA 510(k) clearance?

SRD-2 received FDA 510(k) clearance on 1978-10-27, under 510(k) number K781646.

Who is the listed applicant for SRD-2?

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 SRD-2?

The FDA product code for SRD-2 is JQW.

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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.

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