FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TUBE, INHALER OXYGEN

K Number: K935582 · Decision Jan 14, 1994
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
87
Applicant Total
24
Review Days
57

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Basic Information

Device Name
TUBE, INHALER OXYGEN
K Number
K935582
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5975
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Puritas Health Care, Inc.
Date Received
November 18, 1993
Decision Date
January 14, 1994
Product Code
BZO
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BZO Set, Tubing And Support, Ventilator (W Harness)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BZO), ordered by most recent decision date.

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Other Clearances by Puritas Health Care, Inc.

K Number Device Name
K942339 SKIN NEUVEAU SCAR TREATMENT
K941197 SILK*SKIN SCAR TREATMENT
K935600 TRACHEAL SUCTION CATHETER
K935531 OP-FLEX SUMP SUCTION SET WITH DIFFUSER TIP
K940074 Y-TYPE BLOOD ADMINISTRATION SET
K940055 MULTISET
K940054 MEASURED VOLUME SOLUTION ADMINISTRATION SET
K935583 SUCTION SET, TRACHAEL
K940056 WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM
K935532 TRANSFER SET
Search all 24 clearances from Puritas Health Care, Inc. →