FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MONITOR, CARDIAC, W/BLOOD PRESS.&TEMP

K Number: K772334 · Decision Feb 21, 1978
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
76
Applicant Total
107
Review Days
61

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MONITOR, CARDIAC, W/BLOOD PRESS.&TEMP
K Number
K772334
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1110
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Telectronics, Inc.
Date Received
December 22, 1977
Decision Date
February 21, 1978
Product Code
DSK
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DSK Computer, Blood-Pressure

Similar 510(k) Clearances

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

View all

Other Clearances by Telectronics, Inc.

K Number Device Name
K890895 IMPLANTABLE ADAPTOR 033-380
K891231 OPTIMA MPT AND SPT PACEMAKERS
K890350 VS-1 SILICONE IMPLANT LEADS (NEW SERIAL # TUBE)
K884411 OPTIMA MPT AND SPT PACEMAKERS
K884278 IMPLANTABLE ELECTRODE LEADS 033-400,402 AND 436
K881837 OPTIMA MPT SERIES III PACEMAKER, 5281D AND 5282D
K874664 IMPLANTABLE ELECTRODE LEAD, MODEL 030-446
K864712 MODEL 1740 PERSONAL POCKET PROGRAMMER
K872766 IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS
K865098 SLIMLINE UNIPOLAR ENDOCARDIAL PACING LEAD, 030-438
Search all 107 clearances from Telectronics, Inc. →