Atlas FDA

BE #16 - MANIFOLD

FDA 510(k) clearance K823481 · decided 1982-12-22

Clearance details

K-number
K823481
Device name
BE #16 - MANIFOLD
Applicant
Instrumentation Industries, Inc.
Decision
Substantially Equivalent
Date received
1982-11-23
Decision date
1982-12-22
Days to decision
29 days
Clearance type
Traditional
Product code
BZO
Device class
1
Regulation number
868.5975
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Mchenry, IL, 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
UNICOR, INC. CORRUGATED TUBING (K953784)Unicor, Inc.1995-09-19
UNICOR, INC. VENTILATOR HOSES (K953785)Unicor, Inc.1995-09-18
PRIMA VENTILATOR HOSES (K952010)Prima, Inc.1995-05-22
PRIMA VOLUMN VENTILATORSS (K952022)Prima, Inc.1995-05-22
PRIMA CUSTOM ANESTESIA CIRCUIT (K952012)Prima, Inc.1995-05-22
PRIMA BREATHING BAGS (K952011)Prima, Inc.1995-05-22
INFANT FLOW SYSTEM (K945740)Hamilton Medical, Inc.1995-03-23
PRIMA, INC. CORRUGATED TUBING (K944531)Prima, Inc.1994-12-02
VENTILATOR HOSE (K942569)Med-Plastics Intl., Inc.1994-06-10
VOLUME VENTILATOR (K942572)Med-Plastics Intl., Inc.1994-06-10
TUBE, INHALER OXYGEN (K935582)Puritas Health Care, Inc.1994-01-14
STAR BREATHING CIRCUITS (K934753)Infrasonics Corp.1993-10-27

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ENDOTRACHEAL TUBE CHANGERS (P800068/S002)Instrumentation Industries, Inc.1999-11-04
ENDOTRACHEAL TUBE CHANGER (P800068/S001)Instrumentation Industries, Inc.1999-07-23
ENDOTRACHEAL TUBE CHANGER (P800068)Instrumentation Industries, Inc.1981-07-21