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FDA 510(k)

MEDILASE SERIES 2200 ENDOSCOPE

K-Number: K901464 · 1990-08-07

ApplicantMedical Laser, Inc.
Decision Date1990-08-07
Product CodeGCM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDILASE SERIES 2200 ENDOSCOPE 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 1990-08-07 under 510(k) number K901464. The device is classified under product code GCM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILASE SERIES 2200 ENDOSCOPE?

MEDILASE SERIES 2200 ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1990-08-07. The listed applicant is Medical Laser, Inc.. The 510(k) number is K901464.

When did MEDILASE SERIES 2200 ENDOSCOPE receive FDA 510(k) clearance?

MEDILASE SERIES 2200 ENDOSCOPE received FDA 510(k) clearance on 1990-08-07, under 510(k) number K901464.

Who is the listed applicant for MEDILASE SERIES 2200 ENDOSCOPE?

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 MEDILASE SERIES 2200 ENDOSCOPE?

The FDA product code for MEDILASE SERIES 2200 ENDOSCOPE is GCM.

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.

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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.

K913136LASER ENDOSCOPE DISC DECOMPRESSION KITSK912265MEDILASE SEMI-RIGID INSTROD SHEATH SERIES AE1000K912447SERIES 5000 ENDOSCOPE CONSOLE MODELS 5100 AND 5200K912089MODIFIED SERIES 2100 ENDOSCOPESK900894MEDILASE SERIES 2100 ENDOSCOPEK900380MEDILASE 5010 ENDOSCOPE CONSOLE

View all 8 devices →

Related Devices (Code: GCM)

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.

K203226TELESCOPE 0 O 10MM WL 305MM / TELESCOPE 30 O 10MM WL 305MM / TELESCOPE 50 O 10MM WL 305MM, TELESCOPE 0 O 10MM WL 440MM / TELESCOPE 30 O 10MM WL 440MM / TELESCOPE 50 O 10MM WL 440MMRichard Wolf Medical Instruments CorporationK083840MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPEMsi Medserv International Deutschland GmbHK001217INSIDE VIEWMonadnock Optics, Inc.K993103ENDOSCOPES,10MM DIAMETER 0 DEGREES; ENDOSCOPES, 10MM DIAMETER, 30 DEGREES; ENDOSCOPES, 10MM DIAMETER, 50 DEGREESRichard Wolf Medical Instruments Corp.K993445OMNISONIC ENDOSCOPIC DEFLECTOROmnisonics Medical TechnologiesK962393KSEA SET FOR ENDOSCOPIC ASSISTED INTUBATIONKARL STORZ Endoscopy-America, 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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