Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DAVIS+GECK ABSORBABLE LIGATING DEVICE

K-Number: K925602 · 1993-07-08

Decision Date1993-07-08
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAVIS+GECK ABSORBABLE LIGATING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K925602. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 45 devices →

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.

↑