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FDA 510(k)

DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S

K-Number: K895473 · 1989-12-08

ApplicantMedical Devices, Inc.
Decision Date1989-12-08
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1989-12-08 under 510(k) number K895473. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S?

DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S is a medical device that received FDA 510(k) clearance on 1989-12-08. The listed applicant is Medical Devices, Inc.. The 510(k) number is K895473.

When did DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S receive FDA 510(k) clearance?

DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S received FDA 510(k) clearance on 1989-12-08, under 510(k) number K895473.

Who is the listed applicant for DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S?

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

What is the FDA product code for DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S?

The FDA product code for DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S is GZJ.

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Other records listing Medical Devices, Inc. as applicant

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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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