PARAPAC 200D TRANSPORT, MODEL V200D
K-Number: K030803 · 2003-09-29
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Device Summary
Frequently Asked Questions
What is the PARAPAC 200D TRANSPORT, MODEL V200D?
PARAPAC 200D TRANSPORT, MODEL V200D is a medical device that received FDA 510(k) clearance on 2003-09-29. The listed applicant is Pneupac , Ltd.. The 510(k) number is K030803.
When did PARAPAC 200D TRANSPORT, MODEL V200D receive FDA 510(k) clearance?
PARAPAC 200D TRANSPORT, MODEL V200D received FDA 510(k) clearance on 2003-09-29, under 510(k) number K030803.
Who is the listed applicant for PARAPAC 200D TRANSPORT, MODEL V200D?
The FDA 510(k) record lists Pneupac , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PARAPAC 200D TRANSPORT, MODEL V200D?
The FDA product code for PARAPAC 200D TRANSPORT, MODEL V200D is BTL.
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 Pneupac , Ltd. 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: BTL)
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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