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FDA 510(k)

2, 3 AND 4 BANDAGE COMPRESS

K-Number: K870993 · 1987-03-31

Decision Date1987-03-31
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

2, 3 AND 4 BANDAGE COMPRESS is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Credit Services, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K870993. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2, 3 AND 4 BANDAGE COMPRESS?

2, 3 AND 4 BANDAGE COMPRESS is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Advantage Credit Services, Inc.. The 510(k) number is K870993.

When did 2, 3 AND 4 BANDAGE COMPRESS receive FDA 510(k) clearance?

2, 3 AND 4 BANDAGE COMPRESS received FDA 510(k) clearance on 1987-03-31, under 510(k) number K870993.

Who is the listed applicant for 2, 3 AND 4 BANDAGE COMPRESS?

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

What is the FDA product code for 2, 3 AND 4 BANDAGE COMPRESS?

The FDA product code for 2, 3 AND 4 BANDAGE COMPRESS is EFQ.

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 Advantage Credit Services, 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: EFQ)

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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