510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Robert Bosch Corp.

Mchenry, IL, US

Robert Bosch Corp. appears in FDA device records in Mchenry, IL. FDA records list 21 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
21
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 21 510(k) clearances for Robert Bosch Corp. between 1979 and 1986. The busiest year on record is 1985, with 9. The most recent is 1986, with 6.

Clearances by year, as a table
510(k) clearance decisions for Robert Bosch Corp., by decision year
YearClearances
19791
19845
19859
19866
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K854493ERG 555 COUCH ERGOMETERDRTSubstantially Equivalent
K854492ERG 551 ERGOMETER, BICYCLEDRTSubstantially Equivalent
K854491ERG 550 ERGOMETER BICYCLEDRTSubstantially Equivalent
K853541SP 4Substantially Equivalent for Some Indications
K853154HV-4IPFSubstantially Equivalent for Some Indications
K853271HEARING AID ANALYSIS SYSTEMETWSubstantially Equivalent
K851485DEFI 502LDDSubstantially Equivalent
K840717ECS 502DRTSubstantially Equivalent
K851937SONOMED 4IMISubstantially Equivalent
K850188BOSCH IN THE EAR HEARING AID SUPERSTARESDSubstantially Equivalent
K850186POST AURICULAR HEARING AIDS STAR 33PP, 44,55F &Substantially Equivalent
K850190STAR 66F-AGC-I HEARING AIDESDSubstantially Equivalent
K850189BOSCH STAR 66PP-S HEARING AIDESDSubstantially Equivalent
K850187BOSCH STARR 66PP -HEARING AIDSESDSubstantially Equivalent
K850185BODY HEARING AIDS MT 80 SPESDSubstantially Equivalent
K842804DIADYN 4IPFSubstantially Equivalent
K842803INTERFERENZ 4IPFSubstantially Equivalent
K842805IMPULS 3, IT SELECTORISBSubstantially Equivalent
K842802VACOMED 4ISASubstantially Equivalent
K842801ULTRAMED 11S601IMJSubstantially Equivalent
K790682TONOTEST BLOOD PRESSURE DEVICEUnknown

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain