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)

SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL

K-Number: K872254 · 1987-12-14

ApplicantSurgical Laser Technologies, Inc.
Decision Date1987-12-14
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Laser Technologies, Inc.. It received FDA 510(k) clearance on 1987-12-14 under 510(k) number K872254. The device is classified under product code HHR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL?

SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL is a medical device that received FDA 510(k) clearance on 1987-12-14. The listed applicant is Surgical Laser Technologies, Inc.. The 510(k) number is K872254.

When did SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL receive FDA 510(k) clearance?

SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL received FDA 510(k) clearance on 1987-12-14, under 510(k) number K872254.

Who is the listed applicant for SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL?

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

What is the FDA product code for SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL?

The FDA product code for SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL is HHR.

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 Surgical Laser Technologies, 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.

K042211MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMSK023624SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921K011409SLT LASERPRO CTH HOLMIUM LASER SYSTEMK010041SLT DIFFUSER FIBERK984018HEMOSLEEVE, MODEL 4.0MM, 5.5MMK983050PNEUMATIC CUTTER SYSTEM

View all 51 devices →

Related Devices (Code: HHR)

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.

K881507ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIESHgm Medical Laser Systems, Inc.K871875MODEL 5050 SURGILASER FOR OB-GYN USELasermatic, Inc.K875314GL-35 COLPOSCOPIC LASER SYSTEMLaser Engineering, Inc.K874615LASER CANNISTER FILTERMedical Marketing, Inc.K880591LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USELaser Peripherals, LLCK880930MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASECopper Lasersonics, Inc.

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.

↑