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FDA 510(k)

DYNA SYSTEM

K-Number: K855167 · 1986-03-04

ApplicantParker Laboratories, Inc.
Decision Date1986-03-04
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DYNA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1986-03-04 under 510(k) number K855167. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNA SYSTEM?

DYNA SYSTEM is a medical device that received FDA 510(k) clearance on 1986-03-04. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K855167.

When did DYNA SYSTEM receive FDA 510(k) clearance?

DYNA SYSTEM received FDA 510(k) clearance on 1986-03-04, under 510(k) number K855167.

Who is the listed applicant for DYNA SYSTEM?

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

What is the FDA product code for DYNA SYSTEM?

The FDA product code for DYNA SYSTEM is EGG.

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Related Devices (Code: EGG)

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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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