Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MINUTEMAN CO2 MICROSURG LASER GEN SURG

K-Number: K843519 · 1984-12-07

Decision Date1984-12-07
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINUTEMAN CO2 MICROSURG LASER GEN SURG is the device name listed in this FDA 510(k) record. The listed applicant is American Surgical Laser, Inc.. It received FDA 510(k) clearance on 1984-12-07 under 510(k) number K843519. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINUTEMAN CO2 MICROSURG LASER GEN SURG?

MINUTEMAN CO2 MICROSURG LASER GEN SURG is a medical device that received FDA 510(k) clearance on 1984-12-07. The listed applicant is American Surgical Laser, Inc.. The 510(k) number is K843519.

When did MINUTEMAN CO2 MICROSURG LASER GEN SURG receive FDA 510(k) clearance?

MINUTEMAN CO2 MICROSURG LASER GEN SURG received FDA 510(k) clearance on 1984-12-07, under 510(k) number K843519.

Who is the listed applicant for MINUTEMAN CO2 MICROSURG LASER GEN SURG?

The FDA 510(k) record lists American Surgical Laser, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINUTEMAN CO2 MICROSURG LASER GEN SURG?

The FDA product code for MINUTEMAN CO2 MICROSURG LASER GEN SURG is GEY.

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 American Surgical Laser, Inc. 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.

Related Devices (Code: GEY)

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.

↑