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FDA 510(k)

FRAME, UNIVERSAL DAY

K-Number: K781793 · 1978-11-03

ApplicantB.G. Orthopedic Corp.
Decision Date1978-11-03
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FRAME, UNIVERSAL DAY is the device name listed in this FDA 510(k) record. The listed applicant is B.G. Orthopedic Corp.. It received FDA 510(k) clearance on 1978-11-03 under 510(k) number K781793. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRAME, UNIVERSAL DAY?

FRAME, UNIVERSAL DAY is a medical device that received FDA 510(k) clearance on 1978-11-03. The listed applicant is B.G. Orthopedic Corp.. The 510(k) number is K781793.

When did FRAME, UNIVERSAL DAY receive FDA 510(k) clearance?

FRAME, UNIVERSAL DAY received FDA 510(k) clearance on 1978-11-03, under 510(k) number K781793.

Who is the listed applicant for FRAME, UNIVERSAL DAY?

The FDA 510(k) record lists B.G. Orthopedic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRAME, UNIVERSAL DAY?

The FDA product code for FRAME, UNIVERSAL DAY is JEC.

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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.

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