Cleared Traditional

K790033 - HVG-100

K790033 is an FDA 510(k) clearance for HVG-100, manufactured by Elmed, Inc.. The device is a Class 2 Physical Medicine device with product code IPF cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K790033 · Elmed, Inc. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1979
Decision
37d
Days
Class 2
Risk

K790033 is an FDA 510(k) clearance for the HVG-100. Classified as Stimulator, Muscle, Powered (product code IPF), Class II - Special Controls.

Submitted by Elmed, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 9, 1979 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5850 - the FDA physical medicine device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Elmed, Inc. devices

FDA 510(k) Submission Details - K790033

510(k) Number K790033 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 03, 1979
Decision Date February 09, 1979
Days to Decision 37 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 115d · This submission: 37d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IPF Device Classification - Class 2, Special Controls

Product Code IPF Stimulator, Muscle, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5850
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Physical Medicine devices follow this clearance model.

Regulatory Peers - IPF Stimulator, Muscle, Powered

All 165
Devices cleared under the same product code (IPF) and FDA review panel - the closest regulatory comparables to K790033.
ZIMMER ELECTRICAL MUSCLE STIMULATOR
K803064 · Zimmer, Inc. · Dec 1980
INTELECT
K801790 · Chattanooga Group, Inc. · Aug 1980
MOD. 3127 NEUROMUSCULAR STIMULATOR
K800484 · Medtronic Vascular · May 1980
MUSCLE STIMULATOR, ELECTRICAL
K781113 · Rich-Mar Corp. · Sep 1978
STEMPLEX
K781167 · Rich-Mar Corp. · Sep 1978
TECA MODEL SP5/T ELECTRO-THER. STIM.
K761220 · Teca, Inc. · Dec 1976