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FDA 510(k)

LARYNGOSCOPE RIGID

K-Number: K882433 · 1988-09-02

Decision Date1988-09-02
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LARYNGOSCOPE RIGID 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 1988-09-02 under 510(k) number K882433. 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 LARYNGOSCOPE RIGID?

LARYNGOSCOPE RIGID is a medical device that received FDA 510(k) clearance on 1988-09-02. The listed applicant is Eastmed Enterprises, Inc.. The 510(k) number is K882433.

When did LARYNGOSCOPE RIGID receive FDA 510(k) clearance?

LARYNGOSCOPE RIGID received FDA 510(k) clearance on 1988-09-02, under 510(k) number K882433.

Who is the listed applicant for LARYNGOSCOPE RIGID?

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 LARYNGOSCOPE RIGID?

The FDA product code for LARYNGOSCOPE RIGID 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

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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