STANDARD RUBBER DAM WITH OR WITHOUT FRAMES
K-Number: K905470 · 1991-04-25
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Device Summary
Frequently Asked Questions
What is the STANDARD RUBBER DAM WITH OR WITHOUT FRAMES?
STANDARD RUBBER DAM WITH OR WITHOUT FRAMES is a medical device that received FDA 510(k) clearance on 1991-04-25. The listed applicant is Elastomade Accessories Sdn Bhd. The 510(k) number is K905470.
When did STANDARD RUBBER DAM WITH OR WITHOUT FRAMES receive FDA 510(k) clearance?
STANDARD RUBBER DAM WITH OR WITHOUT FRAMES received FDA 510(k) clearance on 1991-04-25, under 510(k) number K905470.
Who is the listed applicant for STANDARD RUBBER DAM WITH OR WITHOUT FRAMES?
The FDA 510(k) record lists Elastomade Accessories Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STANDARD RUBBER DAM WITH OR WITHOUT FRAMES?
The FDA product code for STANDARD RUBBER DAM WITH OR WITHOUT FRAMES is EIE.
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 Elastomade Accessories Sdn Bhd 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: EIE)
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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