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FDA 510(k)

MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE)

K-Number: K901489 · 1990-04-10

Decision Date1990-04-10
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE) 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 1990-04-10 under 510(k) number K901489. 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 MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE)?

MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE) is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Eastmed Enterprises, Inc.. The 510(k) number is K901489.

When did MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE) receive FDA 510(k) clearance?

MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE) received FDA 510(k) clearance on 1990-04-10, under 510(k) number K901489.

Who is the listed applicant for MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE)?

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 MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE)?

The FDA product code for MACINTOSH LARYNGOSCOPE BLADES (AMERICAN PROFILE) is CCW.

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 Eastmed Enterprises, Inc. 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 13 devices →

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.

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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