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FDA 510(k)

IODOSORB POWDER

K-Number: K870559 · 1987-03-20

ApplicantPerstorp AB C/O Robert Joel Slomoff
Decision Date1987-03-20
Product CodeKOZ
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

IODOSORB POWDER is the device name listed in this FDA 510(k) record. The listed applicant is Perstorp AB C/O Robert Joel Slomoff. It received FDA 510(k) clearance on 1987-03-20 under 510(k) number K870559. 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 IODOSORB POWDER?

IODOSORB POWDER is a medical device that received FDA 510(k) clearance on 1987-03-20. The listed applicant is Perstorp AB C/O Robert Joel Slomoff. The 510(k) number is K870559.

When did IODOSORB POWDER receive FDA 510(k) clearance?

IODOSORB POWDER received FDA 510(k) clearance on 1987-03-20, under 510(k) number K870559.

Who is the listed applicant for IODOSORB POWDER?

The FDA 510(k) record lists Perstorp AB C/O Robert Joel Slomoff as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IODOSORB POWDER?

The FDA product code for IODOSORB POWDER 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Perstorp AB C/O Robert Joel Slomoff 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.

K905069IODOSORB GEL

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.

K905206INCARE PINSITE DRESSINGHollister, Inc.K905688CUTINOVA HYDROBeiersdorf, Inc.K905069IODOSORB GELPerstorp AB C/O Robert Joel SlomoffK904604REDI-RELEASE ABSORBENT DRESSINGFountain Pharmaceuticals, Inc.K903645DERMASORB WOUND CONTACT LAYER DRESSINGConvatec, A Division of E.R. Squibb & SonsK896828BIOCLUSIVE(R) ABSORBENT DRESSINGJohnson & Johnson International

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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