Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES)

K-Number: K964006 · 1996-12-31

ApplicantHollister, Inc.
Decision Date1996-12-31
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES) is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1996-12-31 under 510(k) number K964006. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES)?

INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES) is a medical device that received FDA 510(k) clearance on 1996-12-31. The listed applicant is Hollister, Inc.. The 510(k) number is K964006.

When did INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES) receive FDA 510(k) clearance?

INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES) received FDA 510(k) clearance on 1996-12-31, under 510(k) number K964006.

Who is the listed applicant for INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES)?

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 INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES)?

The FDA product code for INCARE HOT/ICE SYSTEM BLANKETS (VARIOUS SIZES AND SHAPES) is ILO.

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 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

View all 85 devices →

Related Devices (Code: ILO)

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.

K213097Armory MotionPain Management Technologies, Inc.K083008COOLSKINElbio Co., Ltd.K073675T-PUMP LOCALIZED TEMPERATURE THERAPY PUMPGaymar Industries, Inc.K072152JUNIPER CLN1 DERMAL COOLING DEVICEJuniper Medical, Inc.K070402MODIFICATION TO POLAR CARE 500Breg, Inc.K040317IVC SYSTEMMark H. Friedman

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.

↑