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FDA 510(k)

XYZ PADS

K-Number: K933159 · 1993-12-13

ApplicantAso Corp.
Decision Date1993-12-13
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

XYZ PADS is the device name listed in this FDA 510(k) record. The listed applicant is Aso Corp.. It received FDA 510(k) clearance on 1993-12-13 under 510(k) number K933159. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XYZ PADS?

XYZ PADS is a medical device that received FDA 510(k) clearance on 1993-12-13. The listed applicant is Aso Corp.. The 510(k) number is K933159.

When did XYZ PADS receive FDA 510(k) clearance?

XYZ PADS received FDA 510(k) clearance on 1993-12-13, under 510(k) number K933159.

Who is the listed applicant for XYZ PADS?

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

What is the FDA product code for XYZ PADS?

The FDA product code for XYZ PADS is EFQ.

Other records listing Aso Corp. 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.

Related Devices (Code: EFQ)

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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