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

MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT

K Number: K897133 · Decision Mar 30, 1990
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
57
Applicant Total
21
Review Days
93

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Basic Information

Device Name
MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT
K Number
K897133
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.1100
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Transidyne General Corp.
Date Received
December 27, 1989
Decision Date
March 30, 1990
Product Code
CBT
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
CBT Arterial Blood Sampling Kit

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Other Clearances by Transidyne General Corp.

K Number Device Name
K961217 BODILY FLUID DISPOSAL KIT
K955658 LACERATION TRAY
K950773 PROPHYLAXIS PACK
K950743 ORAL PROCEDURE PACK
K950449 SURGICAL BUR
K950403 SURGICAL SAW BLADES
K924811 I.V. START KIT
K924243 TRACHEOSTOMY CARE KIT
K922339 SUTURE REMOVAL KIT
K922041 PRIMARY SURGICAL DRESSING TRAY
Search all 21 clearances from Transidyne General Corp. →