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FDA 510(k)

HOLLISTER WOUND EXUDATE ABSORBER

K-Number: K820160 · 1982-04-21

ApplicantHollister, Inc.
Decision Date1982-04-21
Product CodeKOZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOLLISTER WOUND EXUDATE ABSORBER is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1982-04-21 under 510(k) number K820160. 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 HOLLISTER WOUND EXUDATE ABSORBER?

HOLLISTER WOUND EXUDATE ABSORBER is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Hollister, Inc.. The 510(k) number is K820160.

When did HOLLISTER WOUND EXUDATE ABSORBER receive FDA 510(k) clearance?

HOLLISTER WOUND EXUDATE ABSORBER received FDA 510(k) clearance on 1982-04-21, under 510(k) number K820160.

Who is the listed applicant for HOLLISTER WOUND EXUDATE ABSORBER?

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

What is the FDA product code for HOLLISTER WOUND EXUDATE ABSORBER?

The FDA product code for HOLLISTER WOUND EXUDATE ABSORBER is KOZ.

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Other records listing Hollister, 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.

K123804INSTAFLO BOWEL CATHETER SYSTEM KITK100273INSTAFLO BOWEL CATHETER SYSTEM KITK090960VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184,K083153ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007K050483EVADRI BLADDER CONTROL SYSTEMSK040779RESTORE WOUND CLEANSER

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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.K896828BIOCLUSIVE(R) ABSORBENT DRESSINGJohnson & Johnson InternationalK903645DERMASORB WOUND CONTACT LAYER DRESSINGConvatec, A Division of E.R. Squibb & Sons

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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