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FDA 510(k)

WELCH ALLYN OPHTHALMOSCOPE

K-Number: K950461 · 1995-04-04

Decision Date1995-04-04
Product CodeHLI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WELCH ALLYN OPHTHALMOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn, Inc.. It received FDA 510(k) clearance on 1995-04-04 under 510(k) number K950461. The device is classified under product code HLI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WELCH ALLYN OPHTHALMOSCOPE?

WELCH ALLYN OPHTHALMOSCOPE is a medical device that received FDA 510(k) clearance on 1995-04-04. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K950461.

When did WELCH ALLYN OPHTHALMOSCOPE receive FDA 510(k) clearance?

WELCH ALLYN OPHTHALMOSCOPE received FDA 510(k) clearance on 1995-04-04, under 510(k) number K950461.

Who is the listed applicant for WELCH ALLYN OPHTHALMOSCOPE?

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

What is the FDA product code for WELCH ALLYN OPHTHALMOSCOPE?

The FDA product code for WELCH ALLYN OPHTHALMOSCOPE is HLI.

Related Clinical Trials

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.

Other records listing Welch Allyn, 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.

View all 109 devices →

Related Devices (Code: HLI)

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.

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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