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FDA 510(k)

USA ASPIRATOR

K-Number: K862751 · 1986-08-04

Decision Date1986-08-04
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

USA ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is U. S. A. Medical Corp.. It received FDA 510(k) clearance on 1986-08-04 under 510(k) number K862751. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the USA ASPIRATOR?

USA ASPIRATOR is a medical device that received FDA 510(k) clearance on 1986-08-04. The listed applicant is U. S. A. Medical Corp.. The 510(k) number is K862751.

When did USA ASPIRATOR receive FDA 510(k) clearance?

USA ASPIRATOR received FDA 510(k) clearance on 1986-08-04, under 510(k) number K862751.

Who is the listed applicant for USA ASPIRATOR?

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

What is the FDA product code for USA ASPIRATOR?

The FDA product code for USA ASPIRATOR is BTA.

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: BTA)

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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