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KEYMED (Medical & Industrial Equipment) Ltd

SOUTHEND-ON-SEA Essex, GB

KEYMED (Medical & Industrial Equipment) Ltd appears in FDA device records in SOUTHEND-ON-SEA Essex, GB. FDA records list 7 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
7
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 7 510(k) clearances for KEYMED (Medical & Industrial Equipment) Ltd between 1988 and 2020. The busiest year on record is 1988, with 1. The most recent is 2020, with 1.

Clearances by year, as a table
510(k) clearance decisions for KEYMED (Medical & Industrial Equipment) Ltd, by decision year
YearClearances
19881
19941
19961
20001
20011
20101
20201
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K193250Irrigation Tubing with CO2 or AirOCXSubstantially Equivalent
K100899OLYMPUS ENDOSCOPIC FLUSHING PUMP, MODEL OPF-2FEQSubstantially Equivalent
K011725OLYMPUS SUCTION PUMP, MODEL KV-5JCXSubstantially Equivalent
K000948OLYMPUS ENDOSCOPIC FLUSHING PUMP MODEL OFP-1FEQSubstantially Equivalent
K962528OLYMPUS MOBILE CHAIR/COUCHFZKSubstantially Equivalent
K930852OLYMPUS SUCTION PUMP MODEL KV-4JCXSubstantially Equivalent
K881478MODIFIED KEYMED FLEXIBLE ESOPHAGEAL DILATORSKNQSubstantially Equivalent

Registered establishments

FDA registered establishments for KEYMED (Medical & Industrial Equipment) Ltd, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
96111741000162602KEYMED (Medical & Industrial Equipment) LtdKeyMed House, SOUTHEND-ON-SEA Essex SS2 5QH GB2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

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

Verification record

There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.

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