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)

DERMATEX STERILE FINGER BANDAGE

K-Number: K833638 · 1983-12-27

Decision Date1983-12-27
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DERMATEX STERILE FINGER BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Dermatec, Inc.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833638. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMATEX STERILE FINGER BANDAGE?

DERMATEX STERILE FINGER BANDAGE is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Dermatec, Inc.. The 510(k) number is K833638.

When did DERMATEX STERILE FINGER BANDAGE receive FDA 510(k) clearance?

DERMATEX STERILE FINGER BANDAGE received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833638.

Who is the listed applicant for DERMATEX STERILE FINGER BANDAGE?

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

What is the FDA product code for DERMATEX STERILE FINGER BANDAGE?

The FDA product code for DERMATEX STERILE FINGER BANDAGE is NAD.

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 Dermatec, 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: NAD)

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.

↑