PULPDENT MALEIC ACID ETCHANTS
K-Number: K932792 · 1993-09-09
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Device Summary
Frequently Asked Questions
What is the PULPDENT MALEIC ACID ETCHANTS?
PULPDENT MALEIC ACID ETCHANTS is a medical device that received FDA 510(k) clearance on 1993-09-09. The listed applicant is Pulpdent Corp.. The 510(k) number is K932792.
When did PULPDENT MALEIC ACID ETCHANTS receive FDA 510(k) clearance?
PULPDENT MALEIC ACID ETCHANTS received FDA 510(k) clearance on 1993-09-09, under 510(k) number K932792.
Who is the listed applicant for PULPDENT MALEIC ACID ETCHANTS?
The FDA 510(k) record lists Pulpdent Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PULPDENT MALEIC ACID ETCHANTS?
The FDA product code for PULPDENT MALEIC ACID ETCHANTS is EBF.
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 Pulpdent Corp. 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: EBF)
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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