MINI-PACK 911 SERIES
K-Number: K912835 · 1992-02-03
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Device Summary
Frequently Asked Questions
What is the MINI-PACK 911 SERIES?
MINI-PACK 911 SERIES is a medical device that received FDA 510(k) clearance on 1992-02-03. The listed applicant is Pace Tech, Inc.. The 510(k) number is K912835.
When did MINI-PACK 911 SERIES receive FDA 510(k) clearance?
MINI-PACK 911 SERIES received FDA 510(k) clearance on 1992-02-03, under 510(k) number K912835.
Who is the listed applicant for MINI-PACK 911 SERIES?
The FDA 510(k) record lists Pace Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINI-PACK 911 SERIES?
The FDA product code for MINI-PACK 911 SERIES is MHX.
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 Pace Tech, 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: MHX)
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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