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FDA 510(k)

THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM

K-Number: K952563 · 1995-07-25

ApplicantThe Tulip Mfg. Co.
Decision Date1995-07-25
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM 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 1995-07-25 under 510(k) number K952563. The device is classified under product code GCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM?

THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1995-07-25. The listed applicant is The Tulip Mfg. Co.. The 510(k) number is K952563.

When did THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM receive FDA 510(k) clearance?

THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM received FDA 510(k) clearance on 1995-07-25, under 510(k) number K952563.

Who is the listed applicant for THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM?

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 LCI-200 ILLUMINATION & IMAGING SYSTEM?

The FDA product code for THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM is GCT.

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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 FORCEPK952951THE TULIP COMPANY BRASON NERVE HOOK & DISSECTORK952953THE TULIP CXOMPANY BRANSON #2 ELEVATOR

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Related Devices (Code: GCT)

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.

K093125ALPHAXENON LIGHT 180 W AND 300 WGimmi GmbHK082925XENON-100 SCB LIGHT SOURCE, MODEL 20132620KARL STORZ Endoscopy-America, Inc.K070376CONMED LINVATEC 300W XENON LIGHT SOURCEConmed LinvatecK040949VIADUCT MINISCOPE AND ACCESSORIESAcueity, Inc.K022490KSEA MEDI PACKKARL STORZ Endoscopy-America, Inc.K031994LINVATEC 300W XENON LIGHT SOURCELinvatec Corp.

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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