Atlas FDA

VENTI-SCAN II

FDA 510(k) clearance K871868 · decided 1988-04-11

Clearance details

K-number
K871868
Device name
VENTI-SCAN II
Applicant
Atomic Products Corp.
Decision
Substantially Equivalent
Date received
1987-05-13
Decision date
1988-04-11
Days to decision
334 days
Clearance type
Traditional
Product code
IYT
Device class
2
Regulation number
892.1390
Medical specialty
Radiology
Advisory committee
Radiology
Location
Shirley, NY, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Atomic Products Corp.

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

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 GAS BREATHING CIRCUIT (K952223)Intertech Resources, Inc.1995-08-11
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

Recalls involving this device

No recalls on record reference this clearance.