CROSS MEDICAL PRODUCT PEDICLE AWL
K-Number: K895587 · 1990-01-04
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Device Summary
Frequently Asked Questions
What is the CROSS MEDICAL PRODUCT PEDICLE AWL?
CROSS MEDICAL PRODUCT PEDICLE AWL is a medical device that received FDA 510(k) clearance on 1990-01-04. The listed applicant is Cross Medical Products, Inc.. The 510(k) number is K895587.
When did CROSS MEDICAL PRODUCT PEDICLE AWL receive FDA 510(k) clearance?
CROSS MEDICAL PRODUCT PEDICLE AWL received FDA 510(k) clearance on 1990-01-04, under 510(k) number K895587.
Who is the listed applicant for CROSS MEDICAL PRODUCT PEDICLE AWL?
The FDA 510(k) record lists Cross Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CROSS MEDICAL PRODUCT PEDICLE AWL?
The FDA product code for CROSS MEDICAL PRODUCT PEDICLE AWL is HWJ.
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 Cross Medical Products, 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: HWJ)
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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