CRONEX COMPACT MAMMOGRAPHY CASSETTE
K-Number: K895335 · 1990-02-16
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Device Summary
Frequently Asked Questions
What is the CRONEX COMPACT MAMMOGRAPHY CASSETTE?
CRONEX COMPACT MAMMOGRAPHY CASSETTE is a medical device that received FDA 510(k) clearance on 1990-02-16. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K895335.
When did CRONEX COMPACT MAMMOGRAPHY CASSETTE receive FDA 510(k) clearance?
CRONEX COMPACT MAMMOGRAPHY CASSETTE received FDA 510(k) clearance on 1990-02-16, under 510(k) number K895335.
Who is the listed applicant for CRONEX COMPACT MAMMOGRAPHY CASSETTE?
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 CRONEX COMPACT MAMMOGRAPHY CASSETTE?
The FDA product code for CRONEX COMPACT MAMMOGRAPHY CASSETTE is IXA.
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: IXA)
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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