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FDA 510(k)

SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID

K-Number: K871514 · 1987-07-09

ApplicantMedical Energy, Inc.
Decision Date1987-07-09
Product CodeLNK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID is the device name listed in this FDA 510(k) record. The listed applicant is Medical Energy, Inc.. It received FDA 510(k) clearance on 1987-07-09 under 510(k) number K871514. The device is classified under product code LNK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID?

SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID is a medical device that received FDA 510(k) clearance on 1987-07-09. The listed applicant is Medical Energy, Inc.. The 510(k) number is K871514.

When did SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID receive FDA 510(k) clearance?

SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID received FDA 510(k) clearance on 1987-07-09, under 510(k) number K871514.

Who is the listed applicant for SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID?

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

What is the FDA product code for SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID?

The FDA product code for SL-100 ND:YAG LASER FOR RECTAL PATHO. & HEMORRHOID is LNK.

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Other records listing Medical Energy, 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.

K041419LIGHTFORCE LF 20/30 980NM SURGICAL DIODE LASER SYSTEMK871512SL-100 ND:YAG LASER FOR GYNECOLOGY USEK871511SL-100 ND:YAG LASER FOR PULMONARY OBSTRUCTIONSK871515SL-100 ND:YAG LASER FOR GASTROINTESTINAL BLEEDINGK871513SL-100 ND:YAG LASER FOR PALLIATION OF GASTRO. MALIK871516SL-100 ND:YAG LASER FOR UROLOGIC SURGERY

View all 7 devices →

Related Devices (Code: LNK)

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.

K925395TECHNOMED PULSOLITH 4000 LASER SYSTEMTeknomed, Inc.K901723MDL-2000 LASERTRIPTERCandela Laser Corp.K874255ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.Minnesota Laser Corp.K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.Minnesota Laser Corp.K880256MODEL 4060 N ND:YAG LASER FOR GASTROENTEROLOGY USESharplan Lasers, Inc.K880193MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USESharplan Lasers, 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.

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