PSI-TEC LIPOSUCTION ASPIRATOR
K-Number: K981215 · 1998-07-01
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Device Summary
Frequently Asked Questions
What is the PSI-TEC LIPOSUCTION ASPIRATOR?
PSI-TEC LIPOSUCTION ASPIRATOR is a medical device that received FDA 510(k) clearance on 1998-07-01. The listed applicant is Byron Medical. The 510(k) number is K981215.
When did PSI-TEC LIPOSUCTION ASPIRATOR receive FDA 510(k) clearance?
PSI-TEC LIPOSUCTION ASPIRATOR received FDA 510(k) clearance on 1998-07-01, under 510(k) number K981215.
Who is the listed applicant for PSI-TEC LIPOSUCTION ASPIRATOR?
The FDA 510(k) record lists Byron Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PSI-TEC LIPOSUCTION ASPIRATOR?
The FDA product code for PSI-TEC LIPOSUCTION ASPIRATOR is QPB.
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 Byron Medical 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: QPB)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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