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FDA 510(k)

THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR

K-Number: K952902 · 1995-11-14

ApplicantThe Tulip Mfg. Co.
Decision Date1995-11-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is The Tulip Mfg. Co.. It received FDA 510(k) clearance on 1995-11-14 under 510(k) number K952902. 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 THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR?

THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR is a medical device that received FDA 510(k) clearance on 1995-11-14. The listed applicant is The Tulip Mfg. Co.. The 510(k) number is K952902.

When did THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR receive FDA 510(k) clearance?

THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR received FDA 510(k) clearance on 1995-11-14, under 510(k) number K952902.

Who is the listed applicant for THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR?

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

What is the FDA product code for THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR?

The FDA product code for THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR is GCJ.

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Other records listing The Tulip Mfg. Co. 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.

K952906THE TULIP LAPAROSCOPE SHEATH 6MM SINGLE STOPCOCKK952959THE TULIP LAPAROSCOPE SHEATH 6MM DUAL STOPCOCKK955502THE TULIP MONO POLAR ROTATABLE METZ SCISSORSK955501THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEPK952932THE TULIP COMPANY BRANSON #1 ELEVATORK952953THE TULIP CXOMPANY BRANSON #2 ELEVATOR

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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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