Bauman Disposable Laryngoscope Blades
FDA 510(k) K905273 · Vital Signs, Inc.
510(k) numberK905273
Submission
- Device name
- Bauman Disposable Laryngoscope Blades
- Applicant
- Vital Signs, Inc.
Totowa, NJ, US - Received
- November 23, 1990
- Decision date
- March 24, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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 Bauman Disposable Laryngoscope Blades cleared by the FDA?
Bauman Disposable Laryngoscope Blades (K905273) received a 510(k) decision of Substantially Equivalent on March 24, 1992, 487 days after the submission was received.
What is the product code of K905273?
The FDA product code is CCW – Laryngoscope, Rigid, a Class I (low risk) device regulated under 21 CFR 868.5540.