FDA 510(k)

ESKA-HERRMANN TRACHEOSTOMY VALVE

K-Number: K871885 · 1987-06-08

Decision Date1987-06-08

Product CodeEWL

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

ESKA-HERRMANN TRACHEOSTOMY VALVE is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1987-06-08 under 510(k) number K871885. The device is classified under product code EWL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESKA-HERRMANN TRACHEOSTOMY VALVE?

ESKA-HERRMANN TRACHEOSTOMY VALVE is a medical device that received FDA 510(k) clearance on 1987-06-08. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K871885.

When did ESKA-HERRMANN TRACHEOSTOMY VALVE receive FDA 510(k) clearance?

ESKA-HERRMANN TRACHEOSTOMY VALVE received FDA 510(k) clearance on 1987-06-08, under 510(k) number K871885.

Who is the listed applicant for ESKA-HERRMANN TRACHEOSTOMY VALVE?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESKA-HERRMANN TRACHEOSTOMY VALVE?

The FDA product code for ESKA-HERRMANN TRACHEOSTOMY VALVE is EWL.

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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.