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FDA 510(k)

PSI-TEC LIPOSUCTION ASPIRATOR

K-Number: K981215 · 1998-07-01

ApplicantByron Medical
Decision Date1998-07-01
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PSI-TEC LIPOSUCTION ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Byron Medical. It received FDA 510(k) clearance on 1998-07-01 under 510(k) number K981215. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 27 devices →

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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