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)

CARE + PLUS SUTURE REMOVAL TRAY

K-Number: K863283 · 1986-09-15

Decision Date1986-09-15
Product Code
DecisionSubstantially Equivalent

Device Summary

CARE + PLUS SUTURE REMOVAL TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Welmed Systems, Inc.. It received FDA 510(k) clearance on 1986-09-15 under 510(k) number K863283. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARE + PLUS SUTURE REMOVAL TRAY?

CARE + PLUS SUTURE REMOVAL TRAY is a medical device that received FDA 510(k) clearance on 1986-09-15. The listed applicant is Welmed Systems, Inc.. The 510(k) number is K863283.

When did CARE + PLUS SUTURE REMOVAL TRAY receive FDA 510(k) clearance?

CARE + PLUS SUTURE REMOVAL TRAY received FDA 510(k) clearance on 1986-09-15, under 510(k) number K863283.

Who is the listed applicant for CARE + PLUS SUTURE REMOVAL TRAY?

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

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 Welmed Systems, 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 7 devices →

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.

↑