BOBCAT
K-Number: K923796 · 1992-11-17
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Device Summary
Frequently Asked Questions
What is the BOBCAT?
BOBCAT is a medical device that received FDA 510(k) clearance on 1992-11-17. The listed applicant is Mobility Mfg. Co.. The 510(k) number is K923796.
When did BOBCAT receive FDA 510(k) clearance?
BOBCAT received FDA 510(k) clearance on 1992-11-17, under 510(k) number K923796.
Who is the listed applicant for BOBCAT?
The FDA 510(k) record lists Mobility Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOBCAT?
The FDA product code for BOBCAT is INI.
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 Mobility Mfg. Co. 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: INI)
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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