Question 1

Who is the manufacturer of LASESONICS LOW POWER CO2 LASER SYSTEM?

Accepted Answer

Heraeus Surgical, Inc. filed the 510(k) submission for LASESONICS LOW POWER CO2 LASER SYSTEM (K953917).

Question 2

What is the FDA product code for LASESONICS LOW POWER CO2 LASER SYSTEM?

Accepted Answer

GEX. It is classified under 21 CFR 878.4810 as a Class 2 device in the General, Plastic Surgery panel.

Question 3

When was LASESONICS LOW POWER CO2 LASER SYSTEM cleared by the FDA?

Accepted Answer

Oct 26, 1995 (decision: SESE).

Question 4

What is the regulatory pathway for LASESONICS LOW POWER CO2 LASER SYSTEM?

Accepted Answer

510(k) clearance (submission type: Traditional).

Question 5

Who can help prepare an FDA 510(k) submission like LASESONICS LOW POWER CO2 LASER SYSTEM?

Accepted Answer

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Record ID	K953917
Device Name	LASESONICS LOW POWER CO2 LASER SYSTEM
Applicant	Heraeus Surgical, Inc.
Product Code	GEX · General, Plastic Surgery
Decision Date	Oct 26, 1995
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 878.4810
Device Class	Class 2

LASESONICS LOW POWER CO2 LASER SYSTEM

Device Facts

Regulatory Classification

Identification