Cleared Traditional

K790930 - TRACHE FITTING M-307

K790930 is an FDA 510(k) clearance for TRACHE FITTING M-307, manufactured by Mem Medical, Inc.. The device is a Class 2 Anesthesiology device with product code BTO cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K790930 · Mem Medical, Inc. · Anesthesiology device
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Jun 1979
Decision
38d
Days
Class 2
Risk

K790930 is an FDA 510(k) clearance for the TRACHE FITTING M-307. Classified as Tube, Tracheostomy (w/wo Connector) (product code BTO), Class II - Special Controls.

Submitted by Mem Medical, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 22, 1979 after a review of 38 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5800 - the FDA anesthesiology and respiratory 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 Mem Medical, Inc. devices

FDA 510(k) Submission Details - K790930

510(k) Number K790930 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 15, 1979
Decision Date June 22, 1979
Days to Decision 38 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
102d faster than avg
Panel avg: 140d · This submission: 38d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTO Device Classification - Class 2, Special Controls

Product Code BTO Tube, Tracheostomy (w/wo Connector)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5800
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - BTO Tube, Tracheostomy (w/wo Connector)

All 59
Devices cleared under the same product code (BTO) and FDA review panel - the closest regulatory comparables to K790930.
SHILEY SINGLE CANNULA TRACHEOSTOMY TUBE
K810106 · Shiley, Inc. · Feb 1981
MONTG. TRACHEAL CANNULA
K802916 · Boston Medical Products, Inc. · Dec 1980
TRACHEOSTOMY CARE KIT
K792069 · National Patent Development Corp. · Oct 1979
TRACHEOSTOMY TUBES, SHORT AND LONG TERM
K791044 · Extracorporeal Medical Specialities, Inc. · Jun 1979
TRACH CARE KIT
K790437 · Abco Dealers, Inc. · Apr 1979
ENDOTRACHEAL TUBE
K772138 · Medline Industries, Inc. · Dec 1977