Robert Bosch Corp.

FDA Regulatory Profile

Robert Bosch Corp. appears in FDA public data with 0 recalls, 21 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 16, 1986.

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K854492ERG 551 ERGOMETER, BICYCLEJune 16, 1986
K854491ERG 550 ERGOMETER BICYCLEJune 16, 1986
K854493ERG 555 COUCH ERGOMETERJune 16, 1986
K853154HV-4March 28, 1986
K853541SP 4March 28, 1986
K853271HEARING AID ANALYSIS SYSTEMJanuary 16, 1986
K851485DEFI 502August 29, 1985
K840717ECS 502August 19, 1985
K851937SONOMED 4July 17, 1985
K850188BOSCH IN THE EAR HEARING AID SUPERSTARApril 9, 1985
K850186POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &March 27, 1985
K850189BOSCH STAR 66PP-S HEARING AIDMarch 25, 1985
K850190STAR 66F-AGC-I HEARING AIDMarch 25, 1985
K850185BODY HEARING AIDS MT 80 SPMarch 25, 1985
K850187BOSCH STARR 66PP -HEARING AIDSMarch 25, 1985
K842803INTERFERENZ 4August 21, 1984
K842804DIADYN 4August 21, 1984
K842802VACOMED 4August 1, 1984
K842805IMPULS 3, IT SELECTORAugust 1, 1984
K842801ULTRAMED 11S601August 1, 1984