SR 301 MEDICAL X-RAY FILM
K-Number: K792317 · 1980-01-09
Advertisement
Device Summary
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.
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.
Advertisement