VERA PD SOLDER
K-Number: K972632 · 1997-08-15
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Device Summary
Frequently Asked Questions
What is the VERA PD SOLDER?
VERA PD SOLDER is a medical device that received FDA 510(k) clearance on 1997-08-15. The listed applicant is Aalba Dent, Inc.. The 510(k) number is K972632.
When did VERA PD SOLDER receive FDA 510(k) clearance?
VERA PD SOLDER received FDA 510(k) clearance on 1997-08-15, under 510(k) number K972632.
Who is the listed applicant for VERA PD SOLDER?
The FDA 510(k) record lists Aalba Dent, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERA PD SOLDER?
The FDA product code for VERA PD SOLDER is EJT.
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 Aalba Dent, 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: EJT)
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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