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FDA 510(k)

RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES

K-Number: K990602 · 1999-07-01

ApplicantTecsa Technical Services
Decision Date1999-07-01
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Tecsa Technical Services. It received FDA 510(k) clearance on 1999-07-01 under 510(k) number K990602. 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 RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES?

RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1999-07-01. The listed applicant is Tecsa Technical Services. The 510(k) number is K990602.

When did RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES receive FDA 510(k) clearance?

RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES received FDA 510(k) clearance on 1999-07-01, under 510(k) number K990602.

Who is the listed applicant for RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES?

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

What is the FDA product code for RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES?

The FDA product code for RICHTER LIPOPLASTY CANNULAS AND ACCESSORIES is QPB.

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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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