'NO-BOIL' VITAMIN B12 KIT
K-Number: K810002 · 1981-01-16
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Device Summary
Frequently Asked Questions
What is the 'NO-BOIL' VITAMIN B12 KIT?
'NO-BOIL' VITAMIN B12 KIT is a medical device that received FDA 510(k) clearance on 1981-01-16. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K810002.
When did 'NO-BOIL' VITAMIN B12 KIT receive FDA 510(k) clearance?
'NO-BOIL' VITAMIN B12 KIT received FDA 510(k) clearance on 1981-01-16, under 510(k) number K810002.
Who is the listed applicant for 'NO-BOIL' VITAMIN B12 KIT?
The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 'NO-BOIL' VITAMIN B12 KIT?
The FDA product code for 'NO-BOIL' VITAMIN B12 KIT is CDD.
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 Diagnostic Products 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: CDD)
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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