Who is the manufacturer of MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY?

Merrimack Laboratories filed the 510(k) submission for MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY (K827506).

What is the regulatory pathway for MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY?

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

Who can help prepare an FDA 510(k) submission like MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY?

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.

MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY

K827506 · Merrimack Laboratories · Jun 11, 1982 · RA

Device Facts

Record ID	K827506
Device Name	MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY
Applicant	Merrimack Laboratories
Decision Date	Jun 11, 1982
Decision	SESE
Submission Type	Traditional

MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY

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