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FDA 510(k)

POLLY'S VITREOUS SCISSORS J-225-S

K-Number: K922355 · 1992-08-18

ApplicantO.R. Specialties, Inc.
Decision Date1992-08-18
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

POLLY'S VITREOUS SCISSORS J-225-S is the device name listed in this FDA 510(k) record. The listed applicant is O.R. Specialties, Inc.. It received FDA 510(k) clearance on 1992-08-18 under 510(k) number K922355. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLLY'S VITREOUS SCISSORS J-225-S?

POLLY'S VITREOUS SCISSORS J-225-S is a medical device that received FDA 510(k) clearance on 1992-08-18. The listed applicant is O.R. Specialties, Inc.. The 510(k) number is K922355.

When did POLLY'S VITREOUS SCISSORS J-225-S receive FDA 510(k) clearance?

POLLY'S VITREOUS SCISSORS J-225-S received FDA 510(k) clearance on 1992-08-18, under 510(k) number K922355.

Who is the listed applicant for POLLY'S VITREOUS SCISSORS J-225-S?

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

What is the FDA product code for POLLY'S VITREOUS SCISSORS J-225-S?

The FDA product code for POLLY'S VITREOUS SCISSORS J-225-S is HQE.

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Other records listing O.R. Specialties, Inc. as applicant

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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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