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FDA 510(k)

ADDITIONAL COMPONENTS KRONNER COMPRES

K-Number: K800502 · 1980-04-02

Decision Date1980-04-02
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADDITIONAL COMPONENTS KRONNER COMPRES is the device name listed in this FDA 510(k) record. The listed applicant is Richard F. Kronner, M.D.. It received FDA 510(k) clearance on 1980-04-02 under 510(k) number K800502. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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

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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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