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FDA 510(k)

SUNQUEST INTERNATIONAL

K-Number: K963059 · 1996-08-23

Decision Date1996-08-23
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUNQUEST INTERNATIONAL is the device name listed in this FDA 510(k) record. The listed applicant is Sunquest Intl., Inc.. It received FDA 510(k) clearance on 1996-08-23 under 510(k) number K963059. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNQUEST INTERNATIONAL?

SUNQUEST INTERNATIONAL is a medical device that received FDA 510(k) clearance on 1996-08-23. The listed applicant is Sunquest Intl., Inc.. The 510(k) number is K963059.

When did SUNQUEST INTERNATIONAL receive FDA 510(k) clearance?

SUNQUEST INTERNATIONAL received FDA 510(k) clearance on 1996-08-23, under 510(k) number K963059.

Who is the listed applicant for SUNQUEST INTERNATIONAL?

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

What is the FDA product code for SUNQUEST INTERNATIONAL?

The FDA product code for SUNQUEST INTERNATIONAL is HQY.

Related Clinical Trials

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.

Related Devices (Code: HQY)

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.

Official Source

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