ADSON-BECKMAN RETRACTOR, SPINAL
K-Number: K905445 · 1991-01-25
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Device Summary
Frequently Asked Questions
What is the ADSON-BECKMAN RETRACTOR, SPINAL?
ADSON-BECKMAN RETRACTOR, SPINAL is a medical device that received FDA 510(k) clearance on 1991-01-25. The listed applicant is A. Henniss. The 510(k) number is K905445.
When did ADSON-BECKMAN RETRACTOR, SPINAL receive FDA 510(k) clearance?
ADSON-BECKMAN RETRACTOR, SPINAL received FDA 510(k) clearance on 1991-01-25, under 510(k) number K905445.
Who is the listed applicant for ADSON-BECKMAN RETRACTOR, SPINAL?
The FDA 510(k) record lists A. Henniss as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADSON-BECKMAN RETRACTOR, SPINAL?
The FDA product code for ADSON-BECKMAN RETRACTOR, SPINAL is GZT.
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 A. Henniss 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: GZT)
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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