INSTRUMENT PAD— 510(k) K791864

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K791864 for INSTRUMENT PAD, Substantially Equivalent on 1979-10-17. Applicant: Procter & Gamble Mfg. Co.. Device class: 2.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1979-09-21
Decision date: 1979-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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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.