Atlas FDA

XENON GAS BREATHING CIRCUIT

FDA 510(k) clearance K952223 · decided 1995-08-11

Clearance details

K-number
K952223
Device name
XENON GAS BREATHING CIRCUIT
Applicant
Intertech Resources, Inc.
Decision
Substantially Equivalent
Date received
1995-05-12
Decision date
1995-08-11
Days to decision
91 days
Clearance type
Traditional
Product code
IYT
Device class
2
Regulation number
892.1390
Medical specialty
Radiology
Advisory committee
Radiology
Location
Fort Myers, FL, 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
Pulmonex II Xenon System (132-503) (K253942)Mirion Technologies (Capintec), Inc.2026-07-07
Patient Administration Set (K200916)Cyclomedica Australia Pty, Ltd.2020-09-01
XENON CIRCUIT (K953513)King Systems Corp.1995-11-03
XENON CIRCUIT (K914747)Gibeck, Inc.1992-02-27
TETLEY PATIENT ADMINISTRATION SET (K913416)Tetley Medical , Ltd.1991-10-28
BOLUS XENON CIRCUIT (K912626)Vital Signs, Inc.1991-08-02
AMICI KRYPTON ADMINISTRATION SYSTEM, MODIFICATION (K904684)Amici, Inc.1991-01-14
AMICI XENON ADMINISTRATION SET (K903805)Amici, Inc.1991-01-14
AMICI TRU-FIT SOFT PLASTIC MOUTHPIECE (K903694)Amici, Inc.1990-10-03
DISPOSABLE RESPIRTORY KIT (MP-200) (K896885)Medipart Jerry Alexander1990-02-26
MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133M (K896125)Medipart Jerry Alexander1990-02-01
DISP. RADIOAEROSOL KIT (MP-400-M) TO FIT SHIELD (K896476)Medipart Jerry Alexander1990-01-22

Recalls involving this device

No recalls on record reference this clearance.