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FDA 510(k)

WOODLYN OPERATION MICROSCOPE

K-Number: K931303 · 1993-06-25

ApplicantWoodlyn, Inc.
Decision Date1993-06-25
Product CodeFSO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WOODLYN OPERATION MICROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1993-06-25 under 510(k) number K931303. The device is classified under product code FSO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOODLYN OPERATION MICROSCOPE?

WOODLYN OPERATION MICROSCOPE is a medical device that received FDA 510(k) clearance on 1993-06-25. The listed applicant is Woodlyn, Inc.. The 510(k) number is K931303.

When did WOODLYN OPERATION MICROSCOPE receive FDA 510(k) clearance?

WOODLYN OPERATION MICROSCOPE received FDA 510(k) clearance on 1993-06-25, under 510(k) number K931303.

Who is the listed applicant for WOODLYN OPERATION MICROSCOPE?

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

What is the FDA product code for WOODLYN OPERATION MICROSCOPE?

The FDA product code for WOODLYN OPERATION MICROSCOPE is FSO.

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 Woodlyn, 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 19 devices →

Related Devices (Code: FSO)

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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