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)

LASER ENDOSCOPE DISC DECOMPRESSION KITS

K-Number: K913136 · 1991-11-01

ApplicantMedical Laser, Inc.
Decision Date1991-11-01
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

LASER ENDOSCOPE DISC DECOMPRESSION KITS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Laser, Inc.. It received FDA 510(k) clearance on 1991-11-01 under 510(k) number K913136. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the LASER ENDOSCOPE DISC DECOMPRESSION KITS?

LASER ENDOSCOPE DISC DECOMPRESSION KITS is a medical device that received FDA 510(k) clearance on 1991-11-01. The listed applicant is Medical Laser, Inc.. The 510(k) number is K913136.

When did LASER ENDOSCOPE DISC DECOMPRESSION KITS receive FDA 510(k) clearance?

LASER ENDOSCOPE DISC DECOMPRESSION KITS received FDA 510(k) clearance on 1991-11-01, under 510(k) number K913136.

Who is the listed applicant for LASER ENDOSCOPE DISC DECOMPRESSION KITS?

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

What is the FDA product code for LASER ENDOSCOPE DISC DECOMPRESSION KITS?

The FDA product code for LASER ENDOSCOPE DISC DECOMPRESSION KITS is LRO.

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 Medical 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.

K912265MEDILASE SEMI-RIGID INSTROD SHEATH SERIES AE1000K912447SERIES 5000 ENDOSCOPE CONSOLE MODELS 5100 AND 5200K912089MODIFIED SERIES 2100 ENDOSCOPESK901464MEDILASE SERIES 2200 ENDOSCOPEK900894MEDILASE SERIES 2100 ENDOSCOPEK900380MEDILASE 5010 ENDOSCOPE CONSOLE

View all 8 devices →

Related Devices (Code: LRO)

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.

K213481Medline General Surgery TrayMedline Industries, Inc.K212258Medline Cardiovascular Procedure KitMedline Industries, Inc.K041080SURGICAL DRAPE KIT - D.I.R.R.A. SRLD.I.R.R.A. S.R.L.K030721QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLEBallard Medical ProductsK023276AMSINO TRACHEOSTOMY CARE TRAYAmsino International, Inc.K980137WORLDWIDE MEDICAL TECHNOLOGIES BONE MARROW BIOPSY PROCEDURE TRAYWorldwide Medical Technologies, LLC

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.

↑