TRAVELPAK MODEL AC-102
K-Number: K854509 · 1986-01-28
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Device Summary
Frequently Asked Questions
What is the TRAVELPAK MODEL AC-102?
TRAVELPAK MODEL AC-102 is a medical device that received FDA 510(k) clearance on 1986-01-28. The listed applicant is Travomed, Inc.. The 510(k) number is K854509.
When did TRAVELPAK MODEL AC-102 receive FDA 510(k) clearance?
TRAVELPAK MODEL AC-102 received FDA 510(k) clearance on 1986-01-28, under 510(k) number K854509.
Who is the listed applicant for TRAVELPAK MODEL AC-102?
The FDA 510(k) record lists Travomed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRAVELPAK MODEL AC-102?
The FDA product code for TRAVELPAK MODEL AC-102 is CAW.
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 Travomed, 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: CAW)
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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