FDA 510(k)

SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT

K-Number: K844051 · 1985-01-18

ApplicantWashington-Greene County Branch Pennsylvania Assoc

Decision Date1985-01-18

Product CodeNXA

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Washington-Greene County Branch Pennsylvania Assoc. It received FDA 510(k) clearance on 1985-01-18 under 510(k) number K844051. The device is classified under product code NXA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT?

SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT is a medical device that received FDA 510(k) clearance on 1985-01-18. The listed applicant is Washington-Greene County Branch Pennsylvania Assoc. The 510(k) number is K844051.

When did SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT receive FDA 510(k) clearance?

SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT received FDA 510(k) clearance on 1985-01-18, under 510(k) number K844051.

Who is the listed applicant for SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT?

The FDA 510(k) record lists Washington-Greene County Branch Pennsylvania Assoc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT?

The FDA product code for SKILCRAFT - TRACHEOTOMY CARE KIT 3 COMPARTMENT is NXA.

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Official Source

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