TOTAL/IGE THEOPHYLLINE CONTROL SERA
K-Number: K870151 · 1987-03-12
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Device Summary
Frequently Asked Questions
What is the TOTAL/IGE THEOPHYLLINE CONTROL SERA?
TOTAL/IGE THEOPHYLLINE CONTROL SERA is a medical device that received FDA 510(k) clearance on 1987-03-12. The listed applicant is 3M Company. The 510(k) number is K870151.
When did TOTAL/IGE THEOPHYLLINE CONTROL SERA receive FDA 510(k) clearance?
TOTAL/IGE THEOPHYLLINE CONTROL SERA received FDA 510(k) clearance on 1987-03-12, under 510(k) number K870151.
Who is the listed applicant for TOTAL/IGE THEOPHYLLINE CONTROL SERA?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TOTAL/IGE THEOPHYLLINE CONTROL SERA?
The FDA product code for TOTAL/IGE THEOPHYLLINE CONTROL SERA is JJX.
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 3M Company 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: JJX)
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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