PERMOBIL EXTERIOR
K-Number: K790858 · 1979-05-15
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Device Summary
Frequently Asked Questions
What is the PERMOBIL EXTERIOR?
PERMOBIL EXTERIOR is a medical device that received FDA 510(k) clearance on 1979-05-15. The listed applicant is Saab-Scania of America, Inc.. The 510(k) number is K790858.
When did PERMOBIL EXTERIOR receive FDA 510(k) clearance?
PERMOBIL EXTERIOR received FDA 510(k) clearance on 1979-05-15, under 510(k) number K790858.
Who is the listed applicant for PERMOBIL EXTERIOR?
The FDA 510(k) record lists Saab-Scania of America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERMOBIL EXTERIOR?
The FDA product code for PERMOBIL EXTERIOR is ITI.
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 Saab-Scania of America, 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: ITI)
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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