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FDA 510(k)

AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED

K-Number: K914741 · 1992-02-03

ApplicantEastmed Enterprises, Inc.
Decision Date1992-02-03
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Eastmed Enterprises, Inc.. It received FDA 510(k) clearance on 1992-02-03 under 510(k) number K914741. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED?

AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED is a medical device that received FDA 510(k) clearance on 1992-02-03. The listed applicant is Eastmed Enterprises, Inc.. The 510(k) number is K914741.

When did AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED receive FDA 510(k) clearance?

AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED received FDA 510(k) clearance on 1992-02-03, under 510(k) number K914741.

Who is the listed applicant for AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED?

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

What is the FDA product code for AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED?

The FDA product code for AMER PROFILE MILLER LARYNGOSCOPE BLADES, MODIFIED is CCW.

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Other records listing Eastmed Enterprises, Inc. as applicant

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Related Devices (Code: CCW)

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.

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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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