LIGHTCAST II CASTING SYSTEM (MODIFIED)
K-Number: K770133 · 1977-01-26
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Device Summary
Frequently Asked Questions
What is the LIGHTCAST II CASTING SYSTEM (MODIFIED)?
LIGHTCAST II CASTING SYSTEM (MODIFIED) is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Solar Laboratories, Inc.. The 510(k) number is K770133.
When did LIGHTCAST II CASTING SYSTEM (MODIFIED) receive FDA 510(k) clearance?
LIGHTCAST II CASTING SYSTEM (MODIFIED) received FDA 510(k) clearance on 1977-01-26, under 510(k) number K770133.
Who is the listed applicant for LIGHTCAST II CASTING SYSTEM (MODIFIED)?
The FDA 510(k) record lists Solar Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIGHTCAST II CASTING SYSTEM (MODIFIED)?
The FDA product code for LIGHTCAST II CASTING SYSTEM (MODIFIED) is ITG.
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 Solar Laboratories, 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: ITG)
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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