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FDA 510(k)

MODEL 555 010 XY CONVERSION(55010)

K-Number: K960737 · 1996-05-22

Decision Date1996-05-22
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 555 010 XY CONVERSION(55010) is the device name listed in this FDA 510(k) record. The listed applicant is Systems Supply Services, Inc.. It received FDA 510(k) clearance on 1996-05-22 under 510(k) number K960737. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 555 010 XY CONVERSION(55010)?

MODEL 555 010 XY CONVERSION(55010) is a medical device that received FDA 510(k) clearance on 1996-05-22. The listed applicant is Systems Supply Services, Inc.. The 510(k) number is K960737.

When did MODEL 555 010 XY CONVERSION(55010) receive FDA 510(k) clearance?

MODEL 555 010 XY CONVERSION(55010) received FDA 510(k) clearance on 1996-05-22, under 510(k) number K960737.

Who is the listed applicant for MODEL 555 010 XY CONVERSION(55010)?

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

What is the FDA product code for MODEL 555 010 XY CONVERSION(55010)?

The FDA product code for MODEL 555 010 XY CONVERSION(55010) is KPQ.

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: KPQ)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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