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FDA 510(k)

ETB TELESCOPE W/WORKING CHANNEL FOR SEPS

K-Number: K972298 · 1998-01-30

ApplicantThe Altomec Corp.
Decision Date1998-01-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ETB TELESCOPE W/WORKING CHANNEL FOR SEPS is the device name listed in this FDA 510(k) record. The listed applicant is The Altomec Corp.. It received FDA 510(k) clearance on 1998-01-30 under 510(k) number K972298. 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 ETB TELESCOPE W/WORKING CHANNEL FOR SEPS?

ETB TELESCOPE W/WORKING CHANNEL FOR SEPS is a medical device that received FDA 510(k) clearance on 1998-01-30. The listed applicant is The Altomec Corp.. The 510(k) number is K972298.

When did ETB TELESCOPE W/WORKING CHANNEL FOR SEPS receive FDA 510(k) clearance?

ETB TELESCOPE W/WORKING CHANNEL FOR SEPS received FDA 510(k) clearance on 1998-01-30, under 510(k) number K972298.

Who is the listed applicant for ETB TELESCOPE W/WORKING CHANNEL FOR SEPS?

The FDA 510(k) record lists The Altomec Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ETB TELESCOPE W/WORKING CHANNEL FOR SEPS?

The FDA product code for ETB TELESCOPE W/WORKING CHANNEL FOR SEPS is GCJ.

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 The Altomec Corp. 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.

K990894ETB TROCAR SYSTEM

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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