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FDA 510(k)

DEBRISAN ABSORBENT PAD

K-Number: K872453 · 1988-01-14

Decision Date1988-01-14
Product CodeKOZ
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

DEBRISAN ABSORBENT PAD is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1988-01-14 under 510(k) number K872453. The device is classified under product code KOZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DEBRISAN ABSORBENT PAD?

DEBRISAN ABSORBENT PAD is a medical device that received FDA 510(k) clearance on 1988-01-14. The listed applicant is Pharmacia, Inc.. The 510(k) number is K872453.

When did DEBRISAN ABSORBENT PAD receive FDA 510(k) clearance?

DEBRISAN ABSORBENT PAD received FDA 510(k) clearance on 1988-01-14, under 510(k) number K872453.

Who is the listed applicant for DEBRISAN ABSORBENT PAD?

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

What is the FDA product code for DEBRISAN ABSORBENT PAD?

The FDA product code for DEBRISAN ABSORBENT PAD is KOZ.

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 Pharmacia, 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.

View all 129 devices →

Related Devices (Code: KOZ)

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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