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FDA 510(k)

CONPHAR OTOSCOPE

K-Number: K813305 · 1982-01-19

ApplicantConphar, Inc.
Decision Date1982-01-19
Product CodeERA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CONPHAR OTOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-01-19 under 510(k) number K813305. The device is classified under product code ERA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR OTOSCOPE?

CONPHAR OTOSCOPE is a medical device that received FDA 510(k) clearance on 1982-01-19. The listed applicant is Conphar, Inc.. The 510(k) number is K813305.

When did CONPHAR OTOSCOPE receive FDA 510(k) clearance?

CONPHAR OTOSCOPE received FDA 510(k) clearance on 1982-01-19, under 510(k) number K813305.

Who is the listed applicant for CONPHAR OTOSCOPE?

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

What is the FDA product code for CONPHAR OTOSCOPE?

The FDA product code for CONPHAR OTOSCOPE is ERA.

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Other records listing Conphar, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

View all 122 devices →

Related Devices (Code: ERA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123821AIO HD OTOSCOPEBlue FocusK121326LANTOS 3D EAR SCANNERLantos TechnologiesK110326OSRAM ITOSOsram Sylvania, Inc.K945264OPTUS OTOSCOPESOptus, Inc.K955043WELCH ALLYN BI-OTOSCOPEWelch Allyn, Inc.K952578WELCH ALLY OTOSCOPEWelch Allyn, Inc.

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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