FDA 510(k)

THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP

K-Number: K955501 · 1996-01-17

Decision Date1996-01-17

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP 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 1996-01-17 under 510(k) number K955501. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP?

THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP is a medical device that received FDA 510(k) clearance on 1996-01-17. The listed applicant is The Tulip Mfg. Co.. The 510(k) number is K955501.

When did THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP receive FDA 510(k) clearance?

THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP received FDA 510(k) clearance on 1996-01-17, under 510(k) number K955501.

Who is the listed applicant for THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP?

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 MONO POLAR ROTATABLE ALLIGATOR FORCEP?

The FDA product code for THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP is GEI.

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Other records listing The Tulip Mfg. Co. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.