FDA 510(k)

THE TULIP MONO POLAR ROTATABLE METZ SCISSORS

K-Number: K955502 · 1996-01-17

Decision Date1996-01-17

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

THE TULIP MONO POLAR ROTATABLE METZ SCISSORS 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 K955502. 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 METZ SCISSORS?

THE TULIP MONO POLAR ROTATABLE METZ SCISSORS 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 K955502.

When did THE TULIP MONO POLAR ROTATABLE METZ SCISSORS receive FDA 510(k) clearance?

THE TULIP MONO POLAR ROTATABLE METZ SCISSORS received FDA 510(k) clearance on 1996-01-17, under 510(k) number K955502.

Who is the listed applicant for THE TULIP MONO POLAR ROTATABLE METZ SCISSORS?

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 METZ SCISSORS?

The FDA product code for THE TULIP MONO POLAR ROTATABLE METZ SCISSORS is GEI.

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Other records listing The Tulip Mfg. Co. as applicant

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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.