KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL
K-Number: K860532 · 1986-03-20
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Device Summary
Frequently Asked Questions
What is the KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL?
KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL is a medical device that received FDA 510(k) clearance on 1986-03-20. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K860532.
When did KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL receive FDA 510(k) clearance?
KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL received FDA 510(k) clearance on 1986-03-20, under 510(k) number K860532.
Who is the listed applicant for KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL?
The FDA 510(k) record lists Kerr Corporation (Danbury) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL?
The FDA product code for KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL is ELW.
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 Kerr Corporation (Danbury) 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: ELW)
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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