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)

ACME MEDICAL AESTHETIC ND:YAG LASER

K-Number: K991798 · 2000-03-06

ApplicantAltus Medical
Decision Date2000-03-06
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACME MEDICAL AESTHETIC ND:YAG LASER is the device name listed in this FDA 510(k) record. The listed applicant is Altus Medical. It received FDA 510(k) clearance on 2000-03-06 under 510(k) number K991798. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACME MEDICAL AESTHETIC ND:YAG LASER?

ACME MEDICAL AESTHETIC ND:YAG LASER is a medical device that received FDA 510(k) clearance on 2000-03-06. The listed applicant is Altus Medical. The 510(k) number is K991798.

When did ACME MEDICAL AESTHETIC ND:YAG LASER receive FDA 510(k) clearance?

ACME MEDICAL AESTHETIC ND:YAG LASER received FDA 510(k) clearance on 2000-03-06, under 510(k) number K991798.

Who is the listed applicant for ACME MEDICAL AESTHETIC ND:YAG LASER?

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

What is the FDA product code for ACME MEDICAL AESTHETIC ND:YAG LASER?

The FDA product code for ACME MEDICAL AESTHETIC ND:YAG LASER is GEX. This falls under the Gastroenterology category.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Altus Medical 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.

K003202FAMILY OF ALTUS MEDICAL COOLGLIDE AESTHETIC LASERS, MODELS I & II

Related Devices (Code: GEX)

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.

K254199PicoreMax (PicoreMax)BLUECORE COMPANY Co., Ltd.K252723Dynamis Pro FamilyFotona D.O.O.K241973SmartIPL_NI SystemLumenis Be, Ltd.K261047Dental Diode Laser Device (Laser-Pen)Guilin Kevin Peter Technology Co., Ltd.K261817Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.K261673LED Therapy Device (QLXY-01)Beijing Nubway S&T Co., Ltd.

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.

↑