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FDA 510(k)

QUICKELS QS 100 SYSTEM

K-Number: K954773 · 1996-07-11

ApplicantFerguson Medical
Decision Date1996-07-11
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUICKELS QS 100 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1996-07-11 under 510(k) number K954773. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKELS QS 100 SYSTEM?

QUICKELS QS 100 SYSTEM is a medical device that received FDA 510(k) clearance on 1996-07-11. The listed applicant is Ferguson Medical. The 510(k) number is K954773.

When did QUICKELS QS 100 SYSTEM receive FDA 510(k) clearance?

QUICKELS QS 100 SYSTEM received FDA 510(k) clearance on 1996-07-11, under 510(k) number K954773.

Who is the listed applicant for QUICKELS QS 100 SYSTEM?

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

What is the FDA product code for QUICKELS QS 100 SYSTEM?

The FDA product code for QUICKELS QS 100 SYSTEM is DRX.

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Other records listing Ferguson Medical as applicant

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Related Devices (Code: DRX)

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.

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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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