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FDA 510(k)

AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2

K-Number: K864821 · 1987-02-10

ApplicantReichert-Jung, Inc.
Decision Date1987-02-10
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2 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 1987-02-10 under 510(k) number K864821. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2?

AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2 is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Reichert-Jung, Inc.. The 510(k) number is K864821.

When did AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2 receive FDA 510(k) clearance?

AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2 received FDA 510(k) clearance on 1987-02-10, under 510(k) number K864821.

Who is the listed applicant for AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2?

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 AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2?

The FDA product code for AIRWAY FIBERSCOPES, MODELS LS-9, 0L-1, 0L-2 & PL-2 is EOB.

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.

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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.

K862551FUNS-10, FUNS-11K852994REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11

Related Devices (Code: EOB)

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

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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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