FDA 510(k) Applications Submitted by PELTON & CRANE CO.

FDA 510(k) Number Submission Date Device Name Applicant
K960819 02/29/1996 HELIODENT DS PELTON & CRANE CO.
K962071 05/28/1996 SPIRIT S1/S2 PELTON & CRANE CO.
K945117 10/18/1994 DELTA PELTON & CRANE CO.
K972249 06/16/1997 ORTHOPHOS PLUS AND ORTHOPHOS PLUS/CD PELTON & CRANE CO.
K972168 06/09/1997 SIDEXIS DIGITAL RADIOGRAPHY SYSTEM PELTON & CRANE CO.


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