[Federal Register Volume 59, Number 173 (Thursday, September 8, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: X94-30908]


[[Page Unknown]]

[Federal Register: September 8, 1994]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Parts 874 and 878

[Docket No. 94M-0260]

 

Medical Devices; Proposed Exemptions From Premarket Notification 
for Certain Classified Devices

Correction

    In proposed rule document 94-17705 beginning on page 37378, in the 
issue of Thursday, July 21, 1994, make the following corrections:
    1. On page 37380, in the third column, in the table entitled 
``TABLE 8.--DENTAL DEVICES--Continued'', under the heading ``Device'', 
in the sixth line, ``burr'' should read ``bur''.


Sec. 874.5220  [Corrected]

    2. On page 37386, in the second column, underneath section heading 
Sec. 874.5220, insert
``* * * * *''.

PART 878--[CORRECTED]

    3. On the same page, in the third column, in the authority 
citation, in the fourth line, ``3601'' should read ``360l''.

BILLING CODE 1505-01-D