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FDA 510(k)

EF SYNERGY QUAD

K-Number: K903589 · 1990-11-13

ApplicantRemel Co.
Decision Date1990-11-13
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

EF SYNERGY QUAD is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1990-11-13 under 510(k) number K903589. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EF SYNERGY QUAD?

EF SYNERGY QUAD is a medical device that received FDA 510(k) clearance on 1990-11-13. The listed applicant is Remel Co.. The 510(k) number is K903589.

When did EF SYNERGY QUAD receive FDA 510(k) clearance?

EF SYNERGY QUAD received FDA 510(k) clearance on 1990-11-13, under 510(k) number K903589.

Who is the listed applicant for EF SYNERGY QUAD?

The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EF SYNERGY QUAD?

The FDA product code for EF SYNERGY QUAD is JWY.

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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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