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FDA 510(k)

IODOSORB GEL

K-Number: K905069 · 1991-01-31

ApplicantPerstorp AB C/O Robert Joel Slomoff
Decision Date1991-01-31
Product CodeKOZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IODOSORB GEL 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 1991-01-31 under 510(k) number K905069. The device is classified under product code KOZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IODOSORB GEL?

IODOSORB GEL is a medical device that received FDA 510(k) clearance on 1991-01-31. The listed applicant is Perstorp AB C/O Robert Joel Slomoff. The 510(k) number is K905069.

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

IODOSORB GEL received FDA 510(k) clearance on 1991-01-31, under 510(k) number K905069.

Who is the listed applicant for IODOSORB GEL?

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 GEL?

The FDA product code for IODOSORB GEL 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.

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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.

K870559IODOSORB POWDER

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.K904604REDI-RELEASE ABSORBENT DRESSINGFountain Pharmaceuticals, Inc.K896828BIOCLUSIVE(R) ABSORBENT DRESSINGJohnson & Johnson InternationalK903645DERMASORB WOUND CONTACT LAYER DRESSINGConvatec, A Division of E.R. Squibb & SonsK904412ALLEVYN DRESSING CLAIMS CHANGESmith & Nephew United, Inc.

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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