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FDA 510(k)

ASHERMAN CHEST BANDAGE

K-Number: K942757 · 1994-08-01

Decision Date1994-08-01
Product CodeMGP
DecisionSubstantially Equivalent for Some Indications

Device Summary

ASHERMAN CHEST BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Asherman Medical Products, LLC. It received FDA 510(k) clearance on 1994-08-01 under 510(k) number K942757. The device is classified under product code MGP. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ASHERMAN CHEST BANDAGE?

ASHERMAN CHEST BANDAGE is a medical device that received FDA 510(k) clearance on 1994-08-01. The listed applicant is Asherman Medical Products, LLC. The 510(k) number is K942757.

When did ASHERMAN CHEST BANDAGE receive FDA 510(k) clearance?

ASHERMAN CHEST BANDAGE received FDA 510(k) clearance on 1994-08-01, under 510(k) number K942757.

Who is the listed applicant for ASHERMAN CHEST BANDAGE?

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

What is the FDA product code for ASHERMAN CHEST BANDAGE?

The FDA product code for ASHERMAN CHEST BANDAGE 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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