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FDA 510(k)

EAZY COVERS

K-Number: K863853 · 1987-03-06

ApplicantSuperior Medical Products
Decision Date1987-03-06
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EAZY COVERS is the device name listed in this FDA 510(k) record. The listed applicant is Superior Medical Products. It received FDA 510(k) clearance on 1987-03-06 under 510(k) number K863853. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAZY COVERS?

EAZY COVERS is a medical device that received FDA 510(k) clearance on 1987-03-06. The listed applicant is Superior Medical Products. The 510(k) number is K863853.

When did EAZY COVERS receive FDA 510(k) clearance?

EAZY COVERS received FDA 510(k) clearance on 1987-03-06, under 510(k) number K863853.

Who is the listed applicant for EAZY COVERS?

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

What is the FDA product code for EAZY COVERS?

The FDA product code for EAZY COVERS is JAA.

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.

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Other records listing Superior Medical Products as applicant

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.

K890272BAG DECANTER

Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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