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FDA 510(k)

ASPIRATING HANDLE W/BACKFLUSHING CAPAB

K-Number: K832560 · 1984-01-04

ApplicantPrecision Medical Instruments, Inc.
Decision Date1984-01-04
Product Code
DecisionSubstantially Equivalent

Device Summary

ASPIRATING HANDLE W/BACKFLUSHING CAPAB is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical Instruments, Inc.. It received FDA 510(k) clearance on 1984-01-04 under 510(k) number K832560. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATING HANDLE W/BACKFLUSHING CAPAB?

ASPIRATING HANDLE W/BACKFLUSHING CAPAB is a medical device that received FDA 510(k) clearance on 1984-01-04. The listed applicant is Precision Medical Instruments, Inc.. The 510(k) number is K832560.

When did ASPIRATING HANDLE W/BACKFLUSHING CAPAB receive FDA 510(k) clearance?

ASPIRATING HANDLE W/BACKFLUSHING CAPAB received FDA 510(k) clearance on 1984-01-04, under 510(k) number K832560.

Who is the listed applicant for ASPIRATING HANDLE W/BACKFLUSHING CAPAB?

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

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Other records listing Precision Medical Instruments, 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.

K852758INFUSION CANNULAMK830037EXTENSION HANDLE FOR ACUTOME PROBEK791212VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG

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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