FDA 510(k)

RUBIN DISPOSABLE CARTILAGE PLANNER

K-Number: K852577 · 1985-07-09

Decision Date1985-07-09

Product Code

DecisionSubstantially Equivalent

Device Summary

RUBIN DISPOSABLE CARTILAGE PLANNER is the device name listed in this FDA 510(k) record. The listed applicant is Frank F. Rubin. It received FDA 510(k) clearance on 1985-07-09 under 510(k) number K852577. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUBIN DISPOSABLE CARTILAGE PLANNER?

RUBIN DISPOSABLE CARTILAGE PLANNER is a medical device that received FDA 510(k) clearance on 1985-07-09. The listed applicant is Frank F. Rubin. The 510(k) number is K852577.

When did RUBIN DISPOSABLE CARTILAGE PLANNER receive FDA 510(k) clearance?

RUBIN DISPOSABLE CARTILAGE PLANNER received FDA 510(k) clearance on 1985-07-09, under 510(k) number K852577.

Who is the listed applicant for RUBIN DISPOSABLE CARTILAGE PLANNER?

The FDA 510(k) record lists Frank F. Rubin as the applicant. This does not by itself establish the device manufacturer.

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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.