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)

STERILE SUTURE REMOVAL KIT

K-Number: K850325 · 1985-02-26

Decision Date1985-02-26
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE SUTURE REMOVAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Excel Health Care Products. It received FDA 510(k) clearance on 1985-02-26 under 510(k) number K850325. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE SUTURE REMOVAL KIT?

STERILE SUTURE REMOVAL KIT is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Excel Health Care Products. The 510(k) number is K850325.

When did STERILE SUTURE REMOVAL KIT receive FDA 510(k) clearance?

STERILE SUTURE REMOVAL KIT received FDA 510(k) clearance on 1985-02-26, under 510(k) number K850325.

Who is the listed applicant for STERILE SUTURE REMOVAL KIT?

The FDA 510(k) record lists Excel Health Care Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE SUTURE REMOVAL KIT?

The FDA product code for STERILE SUTURE REMOVAL KIT is KDD.

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 Excel Health Care Products 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: KDD)

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.

↑