Bora Up 2080, Bora Up 2080 Op and Bora Up 2080 Mounting

FDA 510(k) K092903 · Maquet GmbH and Co. KG

Substantially Equivalent

510(k) numberK092903

Submission

Device name
Bora Up 2080, Bora Up 2080 Op and Bora Up 2080 Mounting
Applicant
Maquet GmbH and Co. KG
Rastatt De-Bw, DE
Received
September 21, 2009
Decision date
December 1, 2009
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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Questions and answers

When was Bora Up 2080, Bora Up 2080 Op and Bora Up 2080 Mounting cleared by the FDA?

Bora Up 2080, Bora Up 2080 Op and Bora Up 2080 Mounting (K092903) received a 510(k) decision of Substantially Equivalent on December 1, 2009, 71 days after the submission was received.

What is the product code of K092903?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.