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FDA 510(k)

MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY

K-Number: K827506 · 1982-06-11

Decision Date1982-06-11
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY is the device name listed in this FDA 510(k) record. The listed applicant is Merrimack Laboratories. It received FDA 510(k) clearance on 1982-06-11 under 510(k) number K827506. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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

MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY is a medical device that received FDA 510(k) clearance on 1982-06-11. The listed applicant is Merrimack Laboratories. The 510(k) number is K827506.

When did MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY receive FDA 510(k) clearance?

MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY received FDA 510(k) clearance on 1982-06-11, under 510(k) number K827506.

Who is the listed applicant for MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY?

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

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 Merrimack Laboratories 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.

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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