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Ritter GmbH

Schwabmuenchen Bavaria, DE

RITTER GMBH appears in FDA device records in Schwabmuenchen Bavaria, DE. FDA records list 10 510(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
10
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 10 510(k) clearances for Ritter GmbH between 1976 and 1983. The busiest year on record is 1978, with 3. The most recent is 1983, with 3.

Clearances by year, as a table
510(k) clearance decisions for Ritter GmbH, by decision year
YearClearances
19762
19783
19801
19821
19833
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K831245TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANODXNSubstantially Equivalent
K832171SELF CHECK DIGITAL BLOOD PRESS. MONITORDXNSubstantially Equivalent
K831976POWER OPTICEAYSubstantially Equivalent
K823180SA-21 DENTAL UNITEIASubstantially Equivalent
K800084RITTER MODEL J DENTAL CHAIRKLCSubstantially Equivalent
K781101ELECTROSURGICAL UNIT 75GEISubstantially Equivalent
K780293ELECTROSURGICAL UNITHAMSubstantially Equivalent
K772300DENTAL CHAIR, VANGUARDKLCSubstantially Equivalent
K760929ACCUTORQ IIEFBSubstantially Equivalent
K760707RITTER STARLIGHT DENTAL OPERATING LIGHTEAZSubstantially Equivalent

Registered establishments

FDA registered establishments for Ritter GmbH, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30018568013001856801RITTER GMBHKaufbeurer Str. 55, Schwabmuenchen Bavaria 86830 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

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