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FDA 510(k)

PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM.

K-Number: K915804 · 1992-03-20

ApplicantPropper Mfg. Co., Inc.
Decision Date1992-03-20
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM. is the device name listed in this FDA 510(k) record. The listed applicant is Propper Mfg. Co., Inc.. It received FDA 510(k) clearance on 1992-03-20 under 510(k) number K915804. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM.?

PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM. is a medical device that received FDA 510(k) clearance on 1992-03-20. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K915804.

When did PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM. receive FDA 510(k) clearance?

PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM. received FDA 510(k) clearance on 1992-03-20, under 510(k) number K915804.

Who is the listed applicant for PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM.?

The FDA 510(k) record lists Propper Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM.?

The FDA product code for PROPPER LARYNGOSCOPE BLADES W FIBER OPTIC ILLUM. is CCW.

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Other records listing Propper Mfg. Co., Inc. as applicant

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Related Devices (Code: CCW)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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