Brattle Instrument Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K810588SYNCHRONIZER #208April 10, 1981
K802978TRANSCUTANEOUS BLOOD OXYGEN MONITOR #300February 2, 1981
K781681PHIPIOLOGICAL SYNCHRONIZER PART#205October 17, 1978
K770692MONITOR, FETAL, NO. L04-1100April 26, 1977
K770297FETAL MONITOR, PART #100-11009March 9, 1977
K770296FETAL MONITOR, PART #101-11009March 9, 1977
K770295ABDOMINAL ECG PROCESSOR FOR FETAL MONI.March 9, 1977