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)

TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING

K-Number: K983234 · 1998-11-25

Decision Date1998-11-25
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Div. of Ethicon, Inc.. It received FDA 510(k) clearance on 1998-11-25 under 510(k) number K983234. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING?

TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING is a medical device that received FDA 510(k) clearance on 1998-11-25. The listed applicant is Johnson & Johnson Medical, Div. of Ethicon, Inc.. The 510(k) number is K983234.

When did TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING receive FDA 510(k) clearance?

TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING received FDA 510(k) clearance on 1998-11-25, under 510(k) number K983234.

Who is the listed applicant for TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING?

The FDA 510(k) record lists Johnson & Johnson Medical, Div. of Ethicon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING?

The FDA product code for TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING is MGP.

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 Johnson & Johnson Medical, Div. of Ethicon, 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.

Related Devices (Code: MGP)

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.

↑