CHEMLAR
K-Number: K781132 · 1978-08-10
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Device Summary
Frequently Asked Questions
What is the CHEMLAR?
CHEMLAR is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Hi Chem, Inc.. The 510(k) number is K781132.
When did CHEMLAR receive FDA 510(k) clearance?
CHEMLAR received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781132.
Who is the listed applicant for CHEMLAR?
The FDA 510(k) record lists Hi Chem, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHEMLAR?
The FDA product code for CHEMLAR is JFS.
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 Hi Chem, 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: JFS)
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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