VINYL POLYSILOXANE IMPRESSION SYSTEM AND RE'CORD
K-Number: K926033 · 1993-05-05
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Device Summary
Frequently Asked Questions
What is the VINYL POLYSILOXANE IMPRESSION SYSTEM AND RE'CORD?
VINYL POLYSILOXANE IMPRESSION SYSTEM AND RE'CORD is a medical device that received FDA 510(k) clearance on 1993-05-05. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K926033.
When did VINYL POLYSILOXANE IMPRESSION SYSTEM AND RE'CORD receive FDA 510(k) clearance?
VINYL POLYSILOXANE IMPRESSION SYSTEM AND RE'CORD received FDA 510(k) clearance on 1993-05-05, under 510(k) number K926033.
Who is the listed applicant for VINYL POLYSILOXANE IMPRESSION SYSTEM AND RE'CORD?
The FDA 510(k) record lists Harry J. Bosworth Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL POLYSILOXANE IMPRESSION SYSTEM AND RE'CORD?
The FDA product code for VINYL POLYSILOXANE IMPRESSION SYSTEM AND RE'CORD 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 Harry J. Bosworth 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: 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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