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FDA 510(k)

ACCU-BEAM TUBE SET

K-Number: K921208 · 1993-06-01

ApplicantTti Medical
Decision Date1993-06-01
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACCU-BEAM TUBE SET is the device name listed in this FDA 510(k) record. The listed applicant is Tti Medical. It received FDA 510(k) clearance on 1993-06-01 under 510(k) number K921208. 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 ACCU-BEAM TUBE SET?

ACCU-BEAM TUBE SET is a medical device that received FDA 510(k) clearance on 1993-06-01. The listed applicant is Tti Medical. The 510(k) number is K921208.

When did ACCU-BEAM TUBE SET receive FDA 510(k) clearance?

ACCU-BEAM TUBE SET received FDA 510(k) clearance on 1993-06-01, under 510(k) number K921208.

Who is the listed applicant for ACCU-BEAM TUBE SET?

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

What is the FDA product code for ACCU-BEAM TUBE SET?

The FDA product code for ACCU-BEAM TUBE SET is GCJ.

Other records listing Tti Medical 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.

K952006ACCU-BEAM FIBER OPTIC HANDPIECEK951895ACCU-BEAM 300W XENON LIGHT SOURCEK945648ACCU-BEAM C02 LASER HANDPIECEK910978ACCU-BEAM LAPAROSCOPIC SYSTEMK895656ACCU-BEAM WAVEGUIDEK890922ACCU-BEAM YAG FIBER

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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.

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

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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