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)

SILK SUTURES-REVISED LABELING

K-Number: K926168 · 1993-12-17

ApplicantLook, Inc.
Decision Date1993-12-17
Product CodeGAR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILK SUTURES-REVISED LABELING is the device name listed in this FDA 510(k) record. The listed applicant is Look, Inc.. It received FDA 510(k) clearance on 1993-12-17 under 510(k) number K926168. The device is classified under product code GAR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILK SUTURES-REVISED LABELING?

SILK SUTURES-REVISED LABELING is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is Look, Inc.. The 510(k) number is K926168.

When did SILK SUTURES-REVISED LABELING receive FDA 510(k) clearance?

SILK SUTURES-REVISED LABELING received FDA 510(k) clearance on 1993-12-17, under 510(k) number K926168.

Who is the listed applicant for SILK SUTURES-REVISED LABELING?

The FDA 510(k) record lists Look, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILK SUTURES-REVISED LABELING?

The FDA product code for SILK SUTURES-REVISED LABELING is GAR.

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 Look, 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 25 devices →

Related Devices (Code: GAR)

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.

↑