Atlas FDA

MONITOR, CARDIAC, W/BLOOD PRESS.&TEMP

FDA 510(k) clearance K772334 · decided 1978-02-21

Clearance details

K-number
K772334
Device name
MONITOR, CARDIAC, W/BLOOD PRESS.&TEMP
Applicant
Telectronics, Inc.
Decision
Substantially Equivalent
Date received
1977-12-22
Decision date
1978-02-21
Days to decision
61 days
Clearance type
Traditional
Product code
DSK
Device class
2
Regulation number
870.1110
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
TELECTRONICS PASAR MODEL 4171 PG (P850027/S006)Telectronics, Inc.1990-05-09
TELECTRONICS PASAR MODEL 4171 PG (P850027/S003)Telectronics, Inc.1990-03-22
TELECTRONICS PASAR MODEL 4171 PG (P850027/S005)Telectronics, Inc.1990-02-02
TELECTRONICS PASAR MODEL 4171 PG (P850027/S002)Telectronics, Inc.1989-04-18
TELECTRONICS PASAR MODEL 4171 PG (P850027/S001)Telectronics, Inc.1987-03-27
TELECTRONICS PASAR MODEL 4171 PG (P850027)Telectronics, Inc.1986-09-30