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FDA 510(k)

ADJUSTABLE ARM SUPPORT

K-Number: K770065 · 1977-02-02

ApplicantRichard F. Kronner, M.D.
Decision Date1977-02-02
Product CodeIOY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ADJUSTABLE ARM SUPPORT 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 1977-02-02 under 510(k) number K770065. The device is classified under product code IOY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADJUSTABLE ARM SUPPORT?

ADJUSTABLE ARM SUPPORT is a medical device that received FDA 510(k) clearance on 1977-02-02. The listed applicant is Richard F. Kronner, M.D.. The 510(k) number is K770065.

When did ADJUSTABLE ARM SUPPORT receive FDA 510(k) clearance?

ADJUSTABLE ARM SUPPORT received FDA 510(k) clearance on 1977-02-02, under 510(k) number K770065.

Who is the listed applicant for ADJUSTABLE ARM SUPPORT?

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 ADJUSTABLE ARM SUPPORT?

The FDA product code for ADJUSTABLE ARM SUPPORT is IOY.

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 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.

K800502ADDITIONAL COMPONENTS KRONNER COMPRESK770066TIBIAL COMPRESSION FRAM FOR FRACTURES

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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