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FDA 510(k)

BAILEY ASPIRATOR/IRRIGATOR

K-Number: K831584 · 1983-08-12

ApplicantMedical Instrument Development Laboratories, Inc.
Decision Date1983-08-12
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BAILEY ASPIRATOR/IRRIGATOR 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 1983-08-12 under 510(k) number K831584. 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 BAILEY ASPIRATOR/IRRIGATOR?

BAILEY ASPIRATOR/IRRIGATOR is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K831584.

When did BAILEY ASPIRATOR/IRRIGATOR receive FDA 510(k) clearance?

BAILEY ASPIRATOR/IRRIGATOR received FDA 510(k) clearance on 1983-08-12, under 510(k) number K831584.

Who is the listed applicant for BAILEY ASPIRATOR/IRRIGATOR?

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 BAILEY ASPIRATOR/IRRIGATOR?

The FDA product code for BAILEY ASPIRATOR/IRRIGATOR is HQE.

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Other records listing Medical Instrument Development Laboratories, 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.

K102222ULTIMATE VIT ENHAMCER (UVE)K020911MID LABS AUTONOMOUS VIT ENHANCER (AVE)K992943VIT ENHANCERK971067DIGI-INJECTORK950287UNIVIT PROBEK934600MICRODRIVE

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Related Devices (Code: HQE)

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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