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FDA 510(k)

BRIMFIELD PRECISION GRASPER/DISSECTOR

K-Number: K946263 · 1995-01-26

ApplicantSpringfield Surgical Instruments
Decision Date1995-01-26
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BRIMFIELD PRECISION GRASPER/DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Springfield Surgical Instruments. It received FDA 510(k) clearance on 1995-01-26 under 510(k) number K946263. 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 BRIMFIELD PRECISION GRASPER/DISSECTOR?

BRIMFIELD PRECISION GRASPER/DISSECTOR is a medical device that received FDA 510(k) clearance on 1995-01-26. The listed applicant is Springfield Surgical Instruments. The 510(k) number is K946263.

When did BRIMFIELD PRECISION GRASPER/DISSECTOR receive FDA 510(k) clearance?

BRIMFIELD PRECISION GRASPER/DISSECTOR received FDA 510(k) clearance on 1995-01-26, under 510(k) number K946263.

Who is the listed applicant for BRIMFIELD PRECISION GRASPER/DISSECTOR?

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

What is the FDA product code for BRIMFIELD PRECISION GRASPER/DISSECTOR?

The FDA product code for BRIMFIELD PRECISION GRASPER/DISSECTOR is GCJ.

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Other records listing Springfield Surgical Instruments 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.

K953410BRIMFIELD PRECISION ARTICULATING FAN RETRACTORK952785BRIMFIELD PRECISION DETACHABLE SCISSORK942499INSULATED SURGICAL ELECTRODEK941276BRIMFIELD PRECISION SECOND GENERATION GRASPER/DISSECTORK941316BRIMFIELD PRECISION FAN RETRACTORK933388BRIMFIELD PRECISION SCISSOR

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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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