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FDA 510(k)

MINUTEMAN C02 MICROSURG LASER PODIATRY

K-Number: K843518 · 1984-12-07

ApplicantAmerican Surgical Laser, Inc.
Decision Date1984-12-07
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINUTEMAN C02 MICROSURG LASER PODIATRY 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 K843518. 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 C02 MICROSURG LASER PODIATRY?

MINUTEMAN C02 MICROSURG LASER PODIATRY 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 K843518.

When did MINUTEMAN C02 MICROSURG LASER PODIATRY receive FDA 510(k) clearance?

MINUTEMAN C02 MICROSURG LASER PODIATRY received FDA 510(k) clearance on 1984-12-07, under 510(k) number K843518.

Who is the listed applicant for MINUTEMAN C02 MICROSURG LASER PODIATRY?

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 C02 MICROSURG LASER PODIATRY?

The FDA product code for MINUTEMAN C02 MICROSURG LASER PODIATRY is GEY.

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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.

K843515MINUTEMAN CO2 MICROSURGICAL LASER GYNK843517MINUTEMAN CO2 MICROSURG LASER DERMATOL-K843519MINUTEMAN CO2 MICROSURG LASER GEN SURGK843514MINUTEMAN CO2 MICROSURGICAL LASER OTO

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.

K050519ADVANCED TURBO DRIVE SYSTEMLinvatec Corp.K020621ARTHROCARE CONTROLLER; ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; WANDSArthrocare Corp.K012738SYMPHONY GRAFT DELIVERY SYSTEM (GDS)DepuyacromedK972308MEDNEXT 1000 DRILLMednext, Inc.K971941AQUA SPRAYBoyd Industries, Inc.K971782BONE AND MARROW COLLECTION SYSTEM KITBiomedical Ent., Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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