BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK
K-Number: K932823 · 1994-02-17
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Device Summary
Frequently Asked Questions
What is the BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK?
BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Portable Power Systems, Inc.. The 510(k) number is K932823.
When did BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK receive FDA 510(k) clearance?
BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK received FDA 510(k) clearance on 1994-02-17, under 510(k) number K932823.
Who is the listed applicant for BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK?
The FDA 510(k) record lists Portable Power Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK?
The FDA product code for BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK is DXN.
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 Portable Power Systems, 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: DXN)
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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