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FDA 510(k)

REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11

K-Number: K852994 · 1985-07-29

Decision Date1985-07-29
Product CodeCAL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11 is the device name listed in this FDA 510(k) record. The listed applicant is Reichert-Jung, Inc.. It received FDA 510(k) clearance on 1985-07-29 under 510(k) number K852994. The device is classified under product code CAL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11?

REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11 is a medical device that received FDA 510(k) clearance on 1985-07-29. The listed applicant is Reichert-Jung, Inc.. The 510(k) number is K852994.

When did REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11 receive FDA 510(k) clearance?

REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11 received FDA 510(k) clearance on 1985-07-29, under 510(k) number K852994.

Who is the listed applicant for REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11?

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

What is the FDA product code for REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11?

The FDA product code for REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11 is CAL.

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 Reichert-Jung, 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.

Related Devices (Code: CAL)

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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