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FDA 510(k)

2C LENS FOG REDUCTION & CLEANING DEVICE

K-Number: K934528 · 1994-02-16

ApplicantH & C Chemical, Inc.
Decision Date1994-02-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

2C LENS FOG REDUCTION & CLEANING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is H & C Chemical, Inc.. It received FDA 510(k) clearance on 1994-02-16 under 510(k) number K934528. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2C LENS FOG REDUCTION & CLEANING DEVICE?

2C LENS FOG REDUCTION & CLEANING DEVICE is a medical device that received FDA 510(k) clearance on 1994-02-16. The listed applicant is H & C Chemical, Inc.. The 510(k) number is K934528.

When did 2C LENS FOG REDUCTION & CLEANING DEVICE receive FDA 510(k) clearance?

2C LENS FOG REDUCTION & CLEANING DEVICE received FDA 510(k) clearance on 1994-02-16, under 510(k) number K934528.

Who is the listed applicant for 2C LENS FOG REDUCTION & CLEANING DEVICE?

The FDA 510(k) record lists H & C Chemical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 2C LENS FOG REDUCTION & CLEANING DEVICE?

The FDA product code for 2C LENS FOG REDUCTION & CLEANING DEVICE is GCJ.

Related Clinical Trials

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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Other records listing H & C Chemical, 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.

K941134EMC2 LENS FOG REDUCTION SOLUTION & CLEANING KITK941094INSUFFLATION TUBING & FILTER

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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