HAND TOWEL— 510(k) K791926

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K791926 for HAND TOWEL, Substantially Equivalent on 1979-10-17. Applicant: Procter & Gamble Mfg. Co.. Device class: 1.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1979-09-27
Decision date: 1979-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NAB

K946015 — IVALON EXTERNAL SPONGE1995-02-27
K940755 — ISOLYER (4X4, 8PLY)1994-05-02
K931610 — OMNISORB II, NONWOVEN SPONGE, STERILE AND NON1993-06-24
K925590 — MULTI-TRAUMA DRESSING1993-04-08
K926072 — K-BAND AND K-CREPE1993-03-19

More clearances from Procter & Gamble Mfg. Co.

K873036 — ATTENDS INCONTINENT BRIEF1988-01-19
K873457 — SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS1988-01-19
K864673 — UNSCENTED MENSTRUAL PAD1987-01-21
K861863 — MODIFIED PROTECTIVE GARMENT1986-08-11
K862348 — SINGLE-USE PATIENT UNDERPAD1986-07-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.