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FDA 510(k)

CURITY NERVE BLOCK TRAY

K-Number: K903887 · 1990-11-30

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1990-11-30
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CURITY NERVE BLOCK TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1990-11-30 under 510(k) number K903887. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY NERVE BLOCK TRAY?

CURITY NERVE BLOCK TRAY is a medical device that received FDA 510(k) clearance on 1990-11-30. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K903887.

When did CURITY NERVE BLOCK TRAY receive FDA 510(k) clearance?

CURITY NERVE BLOCK TRAY received FDA 510(k) clearance on 1990-11-30, under 510(k) number K903887.

Who is the listed applicant for CURITY NERVE BLOCK TRAY?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURITY NERVE BLOCK TRAY?

The FDA product code for CURITY NERVE BLOCK TRAY is CAZ.

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Other records listing Kendall Healthcare Products Co. Div.Of Tyco Health as applicant

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Related Devices (Code: CAZ)

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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.

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