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FDA 510(k)

DISPOSABLE LARYNGOSCOPE

K-Number: K850437 · 1985-02-14

ApplicantVital Signs, Inc.
Decision Date1985-02-14
Product CodeLLW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1985-02-14 under 510(k) number K850437. The device is classified under product code LLW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE LARYNGOSCOPE?

DISPOSABLE LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1985-02-14. The listed applicant is Vital Signs, Inc.. The 510(k) number is K850437.

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

DISPOSABLE LARYNGOSCOPE received FDA 510(k) clearance on 1985-02-14, under 510(k) number K850437.

Who is the listed applicant for DISPOSABLE LARYNGOSCOPE?

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

What is the FDA product code for DISPOSABLE LARYNGOSCOPE?

The FDA product code for DISPOSABLE LARYNGOSCOPE is LLW.

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Other records listing Vital Signs, Inc. as applicant

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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.

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