KAHN-TACT U.S.A., EFF LARYNGOSCOPE
K-Number: K872480 · 1987-08-10
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Device Summary
Frequently Asked Questions
What is the KAHN-TACT U.S.A., EFF LARYNGOSCOPE?
KAHN-TACT U.S.A., EFF LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1987-08-10. The listed applicant is Effner and Spreine Co.. The 510(k) number is K872480.
When did KAHN-TACT U.S.A., EFF LARYNGOSCOPE receive FDA 510(k) clearance?
KAHN-TACT U.S.A., EFF LARYNGOSCOPE received FDA 510(k) clearance on 1987-08-10, under 510(k) number K872480.
Who is the listed applicant for KAHN-TACT U.S.A., EFF LARYNGOSCOPE?
The FDA 510(k) record lists Effner and Spreine Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KAHN-TACT U.S.A., EFF LARYNGOSCOPE?
The FDA product code for KAHN-TACT U.S.A., EFF LARYNGOSCOPE 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 Effner and Spreine Co. 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: 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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