ADDITIONAL COMPONENTS KRONNER COMPRES
K-Number: K800502 · 1980-04-02
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Device Summary
Frequently Asked Questions
What is the ADDITIONAL COMPONENTS KRONNER COMPRES?
ADDITIONAL COMPONENTS KRONNER COMPRES is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is Richard F. Kronner, M.D.. The 510(k) number is K800502.
When did ADDITIONAL COMPONENTS KRONNER COMPRES receive FDA 510(k) clearance?
ADDITIONAL COMPONENTS KRONNER COMPRES received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800502.
Who is the listed applicant for ADDITIONAL COMPONENTS KRONNER COMPRES?
The FDA 510(k) record lists Richard F. Kronner, M.D. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADDITIONAL COMPONENTS KRONNER COMPRES?
The FDA product code for ADDITIONAL COMPONENTS KRONNER COMPRES is HRS.
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 Richard F. Kronner, M.D. 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: HRS)
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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