DAVIS+GECK ABSORBABLE LIGATING DEVICE
K-Number: K925602 · 1993-07-08
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Device Summary
Frequently Asked Questions
What is the DAVIS+GECK ABSORBABLE LIGATING DEVICE?
DAVIS+GECK ABSORBABLE LIGATING DEVICE is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K925602.
When did DAVIS+GECK ABSORBABLE LIGATING DEVICE receive FDA 510(k) clearance?
DAVIS+GECK ABSORBABLE LIGATING DEVICE received FDA 510(k) clearance on 1993-07-08, under 510(k) number K925602.
Who is the listed applicant for DAVIS+GECK ABSORBABLE LIGATING DEVICE?
The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DAVIS+GECK ABSORBABLE LIGATING DEVICE?
The FDA product code for DAVIS+GECK ABSORBABLE LIGATING DEVICE is GCJ.
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 Davis & Geck, 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: GCJ)
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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