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FDA 510(k)

BRIMFIELD PRECISION SCISSOR

K-Number: K933388 · 1993-10-21

ApplicantSpringfield Surgical Instruments
Decision Date1993-10-21
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BRIMFIELD PRECISION SCISSOR 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 1993-10-21 under 510(k) number K933388. 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 SCISSOR?

BRIMFIELD PRECISION SCISSOR is a medical device that received FDA 510(k) clearance on 1993-10-21. The listed applicant is Springfield Surgical Instruments. The 510(k) number is K933388.

When did BRIMFIELD PRECISION SCISSOR receive FDA 510(k) clearance?

BRIMFIELD PRECISION SCISSOR received FDA 510(k) clearance on 1993-10-21, under 510(k) number K933388.

Who is the listed applicant for BRIMFIELD PRECISION SCISSOR?

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 SCISSOR?

The FDA product code for BRIMFIELD PRECISION SCISSOR 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 SCISSORK946263BRIMFIELD PRECISION GRASPER/DISSECTORK942499INSULATED SURGICAL ELECTRODEK941276BRIMFIELD PRECISION SECOND GENERATION GRASPER/DISSECTORK941316BRIMFIELD PRECISION FAN RETRACTOR

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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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