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FDA 510(k)

BEECHER 20 GA. PROBE

K-Number: K833800 · 1984-01-04

ApplicantBeecher Medical Diagnostic Instrumentation
Decision Date1984-01-04
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BEECHER 20 GA. PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Beecher Medical Diagnostic Instrumentation. It received FDA 510(k) clearance on 1984-01-04 under 510(k) number K833800. 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 BEECHER 20 GA. PROBE?

BEECHER 20 GA. PROBE is a medical device that received FDA 510(k) clearance on 1984-01-04. The listed applicant is Beecher Medical Diagnostic Instrumentation. The 510(k) number is K833800.

When did BEECHER 20 GA. PROBE receive FDA 510(k) clearance?

BEECHER 20 GA. PROBE received FDA 510(k) clearance on 1984-01-04, under 510(k) number K833800.

Who is the listed applicant for BEECHER 20 GA. PROBE?

The FDA 510(k) record lists Beecher Medical Diagnostic Instrumentation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEECHER 20 GA. PROBE?

The FDA product code for BEECHER 20 GA. PROBE is HQC.

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Other records listing Beecher Medical Diagnostic Instrumentation 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.

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Related Devices (Code: HQC)

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.

K261264Stellaris Elite™ vision enhancement system; Posterior and Combined Procedure Pack(s): 23 ga. Posterior Elite™ Pack (SE5423); 23 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423B); 25 ga. Posterior Elite™ Pack (SE5425); 25 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5425B); 27 ga. Bi-Blade™ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5427B); 23 ga. Bi-Blade™+ Vitreous Cutter Posterior Stellaris Elite™ Pack (SE5423BB+); 25 ga. Bi-Blade™+Bausch and LombK252052Stellaris Elite™ vision enhancement system (BL11145, BL14455, BL15455, SE14565, SE15565, SE14565E, SE15565E)Bausch and Lomb, IncorporatedK250501System SophiThis AGK243395MICOR 700 with Auto I/ACarl Zeiss Meditec Cataract Technology, Inc.K242801MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)Carl Zeiss Meditec Cataract Technology, Inc.K240169Stellaris Elite vision enhancement system (BL11145, BL14455, BL15455)Bausch and Lomb, Incorporated

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.

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