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FDA 510(k)

KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT

K-Number: K941493 · 1994-06-22

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1994-06-22
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT 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 1994-06-22 under 510(k) number K941493. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT?

KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT is a medical device that received FDA 510(k) clearance on 1994-06-22. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K941493.

When did KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT receive FDA 510(k) clearance?

KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT received FDA 510(k) clearance on 1994-06-22, under 510(k) number K941493.

Who is the listed applicant for KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT?

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 KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT?

The FDA product code for KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT 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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