BACTIDROP(TM) FERRIC CHLORIDE (10%)
K-Number: K913002 · 1991-09-23
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Device Summary
Frequently Asked Questions
What is the BACTIDROP(TM) FERRIC CHLORIDE (10%)?
BACTIDROP(TM) FERRIC CHLORIDE (10%) is a medical device that received FDA 510(k) clearance on 1991-09-23. The listed applicant is Remel Co.. The 510(k) number is K913002.
When did BACTIDROP(TM) FERRIC CHLORIDE (10%) receive FDA 510(k) clearance?
BACTIDROP(TM) FERRIC CHLORIDE (10%) received FDA 510(k) clearance on 1991-09-23, under 510(k) number K913002.
Who is the listed applicant for BACTIDROP(TM) FERRIC CHLORIDE (10%)?
The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BACTIDROP(TM) FERRIC CHLORIDE (10%)?
The FDA product code for BACTIDROP(TM) FERRIC CHLORIDE (10%) is JTO.
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 Remel Co. 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: JTO)
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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