CRAWLER
K-Number: K841695 · 1984-05-10
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Device Summary
Frequently Asked Questions
What is the CRAWLER?
CRAWLER is a medical device that received FDA 510(k) clearance on 1984-05-10. The listed applicant is Maddak, Inc.. The 510(k) number is K841695.
When did CRAWLER receive FDA 510(k) clearance?
CRAWLER received FDA 510(k) clearance on 1984-05-10, under 510(k) number K841695.
Who is the listed applicant for CRAWLER?
The FDA 510(k) record lists Maddak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRAWLER?
The FDA product code for CRAWLER is KNL.
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 Maddak, 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: KNL)
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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