The following data is part of a premarket notification filed by Procter & Gamble Mfg. Co. with the FDA for Modified Protective Garment.
Device ID | K861863 |
510k Number | K861863 |
Device Name: | MODIFIED PROTECTIVE GARMENT |
Classification | Garment, Protective, For Incontinence |
Applicant | PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati, OH 45201 |
Contact | James T O'reilly |
Correspondent | James T O'reilly PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati, OH 45201 |
Product Code | EYQ |
CFR Regulation Number | 876.5920 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-05-15 |
Decision Date | 1986-08-11 |