510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Fresenius Kabi Deutschland GmbH

BAD HERSFELD Hesse, DE

FRESENIUS KABI DEUTSCHLAND GMBH appears in FDA device records in BAD HERSFELD Hesse, DE. FDA records list one 510(k) clearance, 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
1
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 1 510(k) clearance for Fresenius Kabi Deutschland GmbH in 2006.

Clearances by year, as a table
510(k) clearance decisions for Fresenius Kabi Deutschland GmbH, by decision year
YearClearances
20061
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K060316COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETSLZHSubstantially Equivalent

Registered establishments

FDA registered establishments for Fresenius Kabi Deutschland GmbH, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
96818193000147578FRESENIUS KABI DEUTSCHLAND GMBH5 ROBERT-KOCH-STRASSE, BAD HERSFELD Hesse D-36251 DE2026

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