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)

POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES

K-Number: K903584 · 1990-10-11

ApplicantLook, Inc.
Decision Date1990-10-11
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES is the device name listed in this FDA 510(k) record. The listed applicant is Look, Inc.. It received FDA 510(k) clearance on 1990-10-11 under 510(k) number K903584. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES?

POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES is a medical device that received FDA 510(k) clearance on 1990-10-11. The listed applicant is Look, Inc.. The 510(k) number is K903584.

When did POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES receive FDA 510(k) clearance?

POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES received FDA 510(k) clearance on 1990-10-11, under 510(k) number K903584.

Who is the listed applicant for POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES?

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 POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES?

The FDA product code for POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES is GAW.

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: GAW)

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.

↑