QUALITONE 46PP-AGC-I
K-Number: K913592 · 1991-09-18
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Device Summary
Frequently Asked Questions
What is the QUALITONE 46PP-AGC-I?
QUALITONE 46PP-AGC-I is a medical device that received FDA 510(k) clearance on 1991-09-18. The listed applicant is Qualitone. The 510(k) number is K913592.
When did QUALITONE 46PP-AGC-I receive FDA 510(k) clearance?
QUALITONE 46PP-AGC-I received FDA 510(k) clearance on 1991-09-18, under 510(k) number K913592.
Who is the listed applicant for QUALITONE 46PP-AGC-I?
The FDA 510(k) record lists Qualitone as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUALITONE 46PP-AGC-I?
The FDA product code for QUALITONE 46PP-AGC-I is ESD.
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 Qualitone 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: ESD)
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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