(a) Identification.
         An ophthalmic instrument table is an AC-powered or manual device on which ophthalmic instruments are intended to be placed.
     
    
        
        (b) Classification.
         Class I (general controls). The AC-powered device and the manual device are exempt from the premarket notification procedures in subpart E of  part 807 of this chapter, subject to the limitations in  § 886.9. The manual device is also exempt from the current good manufacturing practice requirements of the quality system regulation in  part 820 of this chapter,  with the exception of  § 820.180, with respect to general requirements concerning records, and  § 820.198, with respect to complaint files.
     
    
        
            Code of Federal Regulations
        
        [55 FR 48443, Nov. 20, 1990, as amended at 59 FR 63014, Dec. 7, 1994; 66 FR 38814, July 25, 2001]