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

Mchenry, IL, US

North American Philips Corp. appears in FDA device records in Mchenry, IL. FDA records list 15 510(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
15
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 15 510(k) clearances for North American Philips Corp. between 1981 and 1984. The busiest year on record is 1981, with 6. The most recent is 1984, with 3.

Clearances by year, as a table
510(k) clearance decisions for North American Philips Corp., by decision year
YearClearances
19816
19821
19835
19843
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K842486ELECTRONIC DIGITAL BP METER HC 3001DXNSubstantially Equivalent
K841489NORELCO ELECTRONIC DIGITAL BP METERUnknown
K833755ELECTRONIC DIGITAL FEVER THERMOMETERFLLSubstantially Equivalent
K830715NORELCO VIBRATING BOARD V900IROSubstantially Equivalent
K830687NORELCO ELECTRONIC ANALOG BLOOD PRESSDXNSubstantially Equivalent
K830686ANEROID BLOOD PRESSURE CUFF #HC1400DXNSubstantially Equivalent
K830685NORELCO DELUXE DIGITAL BLOOD PRESSUREDXNSubstantially Equivalent
K830684NORELCO ELECTRONIC DIGITAL BLOOD PRESSDXNSubstantially Equivalent
K813451UVA FLUORESCENT TANNING LAMPSIOBSubstantially Equivalent
K811891NORELCO MASSAGER PLUS HEAT BELTISASubstantially Equivalent
K811636NORELCO ELECTRONIC BLOOD PRESSURE METERDXNSubstantially Equivalent
K811635NORELCO DIGITAL BLOOD PRESSURE METERDXNSubstantially Equivalent
K811634NORELCO ANEROID BLOOD PRESSURE METERDXQSubstantially Equivalent
K811672NORELCO ELECTRONIC DIGITAL THERMOMETERFLLSubstantially Equivalent
K811188NORELCO BLOOD PRESSURE METERDXNSubstantially Equivalent

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