VIP- VARIABLE INTENSITY POLYMERIZER
K-Number: K000426 · 2000-04-12
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Device Summary
Frequently Asked Questions
What is the VIP- VARIABLE INTENSITY POLYMERIZER?
VIP- VARIABLE INTENSITY POLYMERIZER is a medical device that received FDA 510(k) clearance on 2000-04-12. The listed applicant is Bisco, Inc.. The 510(k) number is K000426.
When did VIP- VARIABLE INTENSITY POLYMERIZER receive FDA 510(k) clearance?
VIP- VARIABLE INTENSITY POLYMERIZER received FDA 510(k) clearance on 2000-04-12, under 510(k) number K000426.
Who is the listed applicant for VIP- VARIABLE INTENSITY POLYMERIZER?
The FDA 510(k) record lists Bisco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIP- VARIABLE INTENSITY POLYMERIZER?
The FDA product code for VIP- VARIABLE INTENSITY POLYMERIZER is EBZ.
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 Bisco, 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: EBZ)
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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