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FDA 510(k)

CREAT BRAND O-RISE GENERAL ASPIRATOR

K-Number: K873940 · 1987-11-25

Decision Date1987-11-25
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CREAT BRAND O-RISE GENERAL ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Aesthetech Corp.. It received FDA 510(k) clearance on 1987-11-25 under 510(k) number K873940. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CREAT BRAND O-RISE GENERAL ASPIRATOR?

CREAT BRAND O-RISE GENERAL ASPIRATOR is a medical device that received FDA 510(k) clearance on 1987-11-25. The listed applicant is Aesthetech Corp.. The 510(k) number is K873940.

When did CREAT BRAND O-RISE GENERAL ASPIRATOR receive FDA 510(k) clearance?

CREAT BRAND O-RISE GENERAL ASPIRATOR received FDA 510(k) clearance on 1987-11-25, under 510(k) number K873940.

Who is the listed applicant for CREAT BRAND O-RISE GENERAL ASPIRATOR?

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

What is the FDA product code for CREAT BRAND O-RISE GENERAL ASPIRATOR?

The FDA product code for CREAT BRAND O-RISE GENERAL 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.

Other records listing Aesthetech 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: 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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