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FDA 510(k)

EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM

K-Number: K882744 · 1988-08-10

ApplicantEffner, Inc.
Decision Date1988-08-10
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM is the device name listed in this FDA 510(k) record. The listed applicant is Effner, Inc.. It received FDA 510(k) clearance on 1988-08-10 under 510(k) number K882744. 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 EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM?

EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM is a medical device that received FDA 510(k) clearance on 1988-08-10. The listed applicant is Effner, Inc.. The 510(k) number is K882744.

When did EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM receive FDA 510(k) clearance?

EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM received FDA 510(k) clearance on 1988-08-10, under 510(k) number K882744.

Who is the listed applicant for EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM?

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

What is the FDA product code for EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM?

The FDA product code for EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM is EOB.

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Other records listing Effner, 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.

K900680EFFNER ARTHROPERISCOPE/ARTHROSCOPE W/REMOV. OPTICSK883830FIBER OPTIC LARYNGOSCOPE

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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