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FDA 510(k)

EXTERNAL NASAL SPLINT

K-Number: K942724 · 1994-07-08

Decision Date1994-07-08
Product CodeEPP
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EXTERNAL NASAL SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Micromed Development Corp.. It received FDA 510(k) clearance on 1994-07-08 under 510(k) number K942724. The device is classified under product code EPP. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTERNAL NASAL SPLINT?

EXTERNAL NASAL SPLINT is a medical device that received FDA 510(k) clearance on 1994-07-08. The listed applicant is Micromed Development Corp.. The 510(k) number is K942724.

When did EXTERNAL NASAL SPLINT receive FDA 510(k) clearance?

EXTERNAL NASAL SPLINT received FDA 510(k) clearance on 1994-07-08, under 510(k) number K942724.

Who is the listed applicant for EXTERNAL NASAL SPLINT?

The FDA 510(k) record lists Micromed Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXTERNAL NASAL SPLINT?

The FDA product code for EXTERNAL NASAL SPLINT is EPP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Micromed Development Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 14 devices →

Related Devices (Code: EPP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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