RTV SILICONE HAND KNEADABLE PUTTY
K-Number: K780778 · 1978-05-31
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Device Summary
Frequently Asked Questions
What is the RTV SILICONE HAND KNEADABLE PUTTY?
RTV SILICONE HAND KNEADABLE PUTTY is a medical device that received FDA 510(k) clearance on 1978-05-31. The listed applicant is Crown Delta Corp.. The 510(k) number is K780778.
When did RTV SILICONE HAND KNEADABLE PUTTY receive FDA 510(k) clearance?
RTV SILICONE HAND KNEADABLE PUTTY received FDA 510(k) clearance on 1978-05-31, under 510(k) number K780778.
Who is the listed applicant for RTV SILICONE HAND KNEADABLE PUTTY?
The FDA 510(k) record lists Crown Delta Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RTV SILICONE HAND KNEADABLE PUTTY?
The FDA product code for RTV SILICONE HAND KNEADABLE PUTTY 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 Crown Delta Corp. 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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