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FDA 510(k)

STERILE CONTINER, X-RAY CASSETTE HOLDER

K-Number: K770903 · 1977-06-29

ApplicantNorth Shore Orthopaedic Group, S.C.
Decision Date1977-06-29
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STERILE CONTINER, X-RAY CASSETTE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is North Shore Orthopaedic Group, S.C.. It received FDA 510(k) clearance on 1977-06-29 under 510(k) number K770903. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE CONTINER, X-RAY CASSETTE HOLDER?

STERILE CONTINER, X-RAY CASSETTE HOLDER is a medical device that received FDA 510(k) clearance on 1977-06-29. The listed applicant is North Shore Orthopaedic Group, S.C.. The 510(k) number is K770903.

When did STERILE CONTINER, X-RAY CASSETTE HOLDER receive FDA 510(k) clearance?

STERILE CONTINER, X-RAY CASSETTE HOLDER received FDA 510(k) clearance on 1977-06-29, under 510(k) number K770903.

Who is the listed applicant for STERILE CONTINER, X-RAY CASSETTE HOLDER?

The FDA 510(k) record lists North Shore Orthopaedic Group, S.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE CONTINER, X-RAY CASSETTE HOLDER?

The FDA product code for STERILE CONTINER, X-RAY CASSETTE HOLDER is IZL.

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Related Devices (Code: IZL)

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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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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