Atlas FDA

IONOTPHORETIC APPLICATOR

FDA 510(k) clearance K781700 · decided 1978-11-03

Clearance details

K-number
K781700
Device name
IONOTPHORETIC APPLICATOR
Applicant
Mcghan Medical Corp.
Decision
Substantially Equivalent
Date received
1978-10-10
Decision date
1978-11-03
Days to decision
24 days
Clearance type
Traditional
Product code
KTB
Device class
2
Regulation number
890.5525
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Walker, MI, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Macroduct Advanced Model 3710 (K180627)Elitechgroup, Inc.2018-07-27
RH-950 (K033192)Iomed, Inc.2003-12-22
NORTHSTAR LIDOCAINE IONTOPHORETIC CONTROLLER (NORTHSTAR CONTROLLER-D) (K031551)Vyteris, Inc.2003-08-20
RH-900 (K031115)Iomed, Inc.2003-07-10
NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM (K010031)Wescor, Inc.2001-03-20
TRANSQ3 (K001522)Iomed, Inc.2000-10-18
PHORESOR MODEL PM2000 (K001410)Iomed, Inc.2000-08-01
Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM (K992874)Wr Medical Electronics Co.1999-11-18
PHORESOR II, MODEL PM900 (K974855)Iomed, Inc.1998-03-27
TRANSQ ELECTRODE PHORESOR II (K954126)Iomed, Inc.1996-01-19
CF INDICATOR MODEL 9800 SWEAT TEST SYSTEM (K895775)Medtronic Vascular1990-04-23
WESCOR MODEL 3700 WEBSTER SWEAT INDUCER (K853973)Wescor, Inc.1985-10-16

Recalls involving this device

No recalls on record reference this clearance.