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FDA 510(k)

LEE SYRINGE

K-Number: K842371 · 1985-01-14

ApplicantPeter F. Lee, Inc.
Decision Date1985-01-14
Product Code
DecisionSubstantially Equivalent

Device Summary

LEE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Peter F. Lee, Inc.. It received FDA 510(k) clearance on 1985-01-14 under 510(k) number K842371. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEE SYRINGE?

LEE SYRINGE is a medical device that received FDA 510(k) clearance on 1985-01-14. The listed applicant is Peter F. Lee, Inc.. The 510(k) number is K842371.

When did LEE SYRINGE receive FDA 510(k) clearance?

LEE SYRINGE received FDA 510(k) clearance on 1985-01-14, under 510(k) number K842371.

Who is the listed applicant for LEE SYRINGE?

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

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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.

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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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