FDA 510(k)

INFUSION SLEEVE - OPHTHALMIC

K-Number: K851009 · 1985-04-03

ApplicantMedical Instrument Development Laboratories, Inc.

Decision Date1985-04-03

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

INFUSION SLEEVE - OPHTHALMIC is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instrument Development Laboratories, Inc.. It received FDA 510(k) clearance on 1985-04-03 under 510(k) number K851009. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFUSION SLEEVE - OPHTHALMIC?

INFUSION SLEEVE - OPHTHALMIC is a medical device that received FDA 510(k) clearance on 1985-04-03. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K851009.

When did INFUSION SLEEVE - OPHTHALMIC receive FDA 510(k) clearance?

INFUSION SLEEVE - OPHTHALMIC received FDA 510(k) clearance on 1985-04-03, under 510(k) number K851009.

Who is the listed applicant for INFUSION SLEEVE - OPHTHALMIC?

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

What is the FDA product code for INFUSION SLEEVE - OPHTHALMIC?

The FDA product code for INFUSION SLEEVE - OPHTHALMIC is HQC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.