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FDA 510(k)

SR 301 MEDICAL X-RAY FILM

K-Number: K792317 · 1980-01-09

Decision Date1980-01-09
Product CodeIWZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SR 301 MEDICAL X-RAY FILM is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1980-01-09 under 510(k) number K792317. The device is classified under product code IWZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SR 301 MEDICAL X-RAY FILM?

SR 301 MEDICAL X-RAY FILM is a medical device that received FDA 510(k) clearance on 1980-01-09. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K792317.

When did SR 301 MEDICAL X-RAY FILM receive FDA 510(k) clearance?

SR 301 MEDICAL X-RAY FILM received FDA 510(k) clearance on 1980-01-09, under 510(k) number K792317.

Who is the listed applicant for SR 301 MEDICAL X-RAY FILM?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SR 301 MEDICAL X-RAY FILM?

The FDA product code for SR 301 MEDICAL X-RAY FILM is IWZ.

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 E.I. Dupont DE Nemours & Co., Inc. 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.

View all 253 devices →

Related Devices (Code: IWZ)

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

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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