Propper Laryngoscope Blades W Fiber Optic Illum.
FDA 510(k) K915804 · Propper Mfg. Co., Inc.
510(k) numberK915804
Submission
- Device name
- Propper Laryngoscope Blades W Fiber Optic Illum.
- Applicant
- Propper Mfg. Co., Inc.
Long Island City, NY, US - Received
- December 24, 1991
- Decision date
- March 20, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- CCW – Laryngoscope, Rigid
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.5540
- Specialty
- Anesthesiology
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Questions and answers
When was Propper Laryngoscope Blades W Fiber Optic Illum. cleared by the FDA?
Propper Laryngoscope Blades W Fiber Optic Illum. (K915804) received a 510(k) decision of Substantially Equivalent on March 20, 1992, 87 days after the submission was received.
What is the product code of K915804?
The FDA product code is CCW – Laryngoscope, Rigid, a Class I (low risk) device regulated under 21 CFR 868.5540.