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Fisher & Paykel Allied Products, Ltd.

Mchenry, IL, US

Fisher & Paykel Allied Products , Ltd. appears in FDA device records in Mchenry, IL. FDA records list 12 510(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
12
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 12 510(k) clearances for Fisher & Paykel Allied Products, Ltd. between 1982 and 1988. The busiest year on record is 1987, with 4. The most recent is 1988, with 1.

Clearances by year, as a table
510(k) clearance decisions for Fisher & Paykel Allied Products, Ltd., by decision year
YearClearances
19821
19831
19841
19853
19861
19874
19881
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K880702MODEL MR430 SPECIAL PURPOSE HUMID. HEATER BASESBTTSubstantially Equivalent
K872138MR630 ENHANCED DUAL SERVO HEATER HUMIDIFIERBTTSubstantially Equivalent
K872139MR420 TRANSPORT HUMIDIFIERBTTSubstantially Equivalent
K863377MR338 SERVO HEATED DELIVERY HUMIDIFIERBTTSubstantially Equivalent
K870055MR590 DUAL HOSE HEATER POWER PACKBTTSubstantially Equivalent
K862923MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIERBTTSubstantially Equivalent
K852962PERIPHERAL NERVE STIMULATOR MODEL A400BXNSubstantially Equivalent
K851879HEATED RESPIRATORY HUMIDIFIERBTTSubstantially Equivalent
K850647HEATED RESPIRATORY HUMIFIFIER MR440BTTSubstantially Equivalent
K843903HEATED RESPIRATORY HUMIDIFIER MR428BTTSubstantially Equivalent
K832928SERVO HEATED RESPIRATORY HUMIDIFIERBTTSubstantially Equivalent
K822816DUAL SERVO HEATED RESPIRATORY HUMIDIFIERBTTSubstantially 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