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FDA 510(k)

ARMAND ENDOSCOPE HOLDER

K-Number: K050051 · 2005-05-16

ApplicantKLS-Martin L.P.
Decision Date2005-05-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARMAND ENDOSCOPE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is KLS-Martin L.P.. It received FDA 510(k) clearance on 2005-05-16 under 510(k) number K050051. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARMAND ENDOSCOPE HOLDER?

ARMAND ENDOSCOPE HOLDER is a medical device that received FDA 510(k) clearance on 2005-05-16. The listed applicant is KLS-Martin L.P.. The 510(k) number is K050051.

When did ARMAND ENDOSCOPE HOLDER receive FDA 510(k) clearance?

ARMAND ENDOSCOPE HOLDER received FDA 510(k) clearance on 2005-05-16, under 510(k) number K050051.

Who is the listed applicant for ARMAND ENDOSCOPE HOLDER?

The FDA 510(k) record lists KLS-Martin L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARMAND ENDOSCOPE HOLDER?

The FDA product code for ARMAND ENDOSCOPE HOLDER is GCJ.

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Other records listing KLS-Martin L.P. 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.

K260137KLS Martin IPS Oral-Max Implants - MR Conditional; Individual Patient Solutions - Ti (IPS-Ti); Individual Patient Solutions - PEEK (IPS-PEEK); KLS Martin Individual Patient SolutionsK254162KLS Martin Ixos SystemK253660KLS Martin Pure Pectus SystemK250988KLS Martin Pure Pectus SystemK250865KLS Martin IPS Forearm SystemK252573KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

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Related Devices (Code: GCJ)

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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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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