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FDA 510(k)

TRIANGULAR BANDAGE

K-Number: K870284 · 1987-02-24

ApplicantThe Medical Group, Inc.
Decision Date1987-02-24
Product Code
DecisionSubstantially Equivalent

Device Summary

TRIANGULAR BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is The Medical Group, Inc.. It received FDA 510(k) clearance on 1987-02-24 under 510(k) number K870284. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIANGULAR BANDAGE?

TRIANGULAR BANDAGE is a medical device that received FDA 510(k) clearance on 1987-02-24. The listed applicant is The Medical Group, Inc.. The 510(k) number is K870284.

When did TRIANGULAR BANDAGE receive FDA 510(k) clearance?

TRIANGULAR BANDAGE received FDA 510(k) clearance on 1987-02-24, under 510(k) number K870284.

Who is the listed applicant for TRIANGULAR BANDAGE?

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

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Other records listing The Medical Group, 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.

K911246THE MEDISCUS PEDCARE MANAGEMENT SYSTEM-MODEL 2K901295PULMONAIR 40 PATIENT MANAGEMENT SYSTEMK881843PEDIATRIC HOSPITAL BEDK881844MAGNUM 800(TM) MANAGEMENT SYSTEMK8702824 X 4 SPONGES, NON-STERILEK8702833 X 3 SPONGES, NON-STERILE

View all 16 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.

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