ENERGIZED DRUG CONTAINER SYSTEM
K-Number: K934119 · 1994-06-09
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Device Summary
Frequently Asked Questions
What is the ENERGIZED DRUG CONTAINER SYSTEM?
ENERGIZED DRUG CONTAINER SYSTEM is a medical device that received FDA 510(k) clearance on 1994-06-09. The listed applicant is Abbott Laboratories. The 510(k) number is K934119.
When did ENERGIZED DRUG CONTAINER SYSTEM receive FDA 510(k) clearance?
ENERGIZED DRUG CONTAINER SYSTEM received FDA 510(k) clearance on 1994-06-09, under 510(k) number K934119.
Who is the listed applicant for ENERGIZED DRUG CONTAINER SYSTEM?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENERGIZED DRUG CONTAINER SYSTEM?
The FDA product code for ENERGIZED DRUG CONTAINER SYSTEM is FPA.
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 Abbott Laboratories 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: FPA)
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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