The following data is part of a premarket notification filed by Gelman Instrument Co. with the FDA for Densitometer 18, Computing, Auto..
Device ID | K772325 |
510k Number | K772325 |
Device Name: | DENSITOMETER 18, COMPUTING, AUTO. |
Classification | Densitometer/scanner (integrating, Reflectance, Tlc, Radiochromat.) Clinica |
Applicant | GELMAN INSTRUMENT CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JQT |
CFR Regulation Number | 862.2400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1977-12-19 |
Decision Date | 1978-01-12 |