Atlas FDA

Carecube Negative Pressure Isolation Chamber

FDA 510(k) clearance K231256 · decided 2024-01-03

Clearance details

K-number
K231256
Device name
Carecube Negative Pressure Isolation Chamber
Applicant
Carecubes, Inc.
Decision
Substantially Equivalent
Date received
2023-05-01
Decision date
2024-01-03
Days to decision
247 days
Clearance type
Traditional
Product code
LGM
Device class
2
Regulation number
880.5450
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
San Francisco, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ORCA (tm) - Operational Rescue Containment Apparatus (K163223)Isovac Products, LLC2017-11-02
PATIENT ISOLATION UNIT, MODEL G019-1000 (K080117)Gentex Corporation2009-01-30
FAILSAFE - PORTABLE INFECTION CONTROL SYSTEMS (K022260)Isolation Systems, Inc.2002-08-29
MTB 1043 TREATMENT BOOTH (K944133)Mark Solutions, Inc.1995-09-07
MICROBACT 12A SYSTEM, 12B SYSTEM, AND 24E SYSTEM (K912444)Radiometer America, Inc.1992-02-18
MODEL 7-AT TREATMENT CHAMBER (K896721)J. H. Emerson Co.1990-01-22
SURGICAL APPAREL, ISOLATION GOWN,MASK,CAP,SLEEVE (K884295)Saybrex Intl., Inc.1988-11-08
INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE (K874306)Busse Hospital Disposables, Inc.1988-03-22
ANAGO ISOLATION MASK (#80-950) (K864116)Anago, Inc.1986-11-25
ISOLATION MASK I.C.S. (K831062)American Threshold Industries, Inc.1983-04-13
STRETCHER TRANSIT ISOLATER #122 (K790657)Vickers America Medical Corp.1979-07-03

Recalls involving this device

No recalls on record reference this clearance.