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FDA 510(k)

BARNES-HIND WETTING & SOAKING SOLUTION

K-Number: K791901 · 1979-11-16

ApplicantBarnes-Hind, Inc.
Decision Date1979-11-16
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BARNES-HIND WETTING & SOAKING SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Barnes-Hind, Inc.. It received FDA 510(k) clearance on 1979-11-16 under 510(k) number K791901. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARNES-HIND WETTING & SOAKING SOLUTION?

BARNES-HIND WETTING & SOAKING SOLUTION is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Barnes-Hind, Inc.. The 510(k) number is K791901.

When did BARNES-HIND WETTING & SOAKING SOLUTION receive FDA 510(k) clearance?

BARNES-HIND WETTING & SOAKING SOLUTION received FDA 510(k) clearance on 1979-11-16, under 510(k) number K791901.

Who is the listed applicant for BARNES-HIND WETTING & SOAKING SOLUTION?

The FDA 510(k) record lists Barnes-Hind, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARNES-HIND WETTING & SOAKING SOLUTION?

The FDA product code for BARNES-HIND WETTING & SOAKING SOLUTION is HQG.

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Other records listing Barnes-Hind, Inc. as applicant

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K852386SOFT MATE AUTOMATIC CONTACT LENS CLEANING UNITK812135BARNES-HIND WEEKLY CLEANERK811554BARNES-HIND SPECTACLE LENS CLEANERK810285BARNES-HIND ROSE BENGAL OPHTHALMIC STR.K800582BARNES-HOND HARD CONTACT LENS STOR. CASEK781007AUTO-CON

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Related Devices (Code: HQG)

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.

K935919SUNGLASSESJa-Ru, Inc.K9207950R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEXOptical Radiation Corp.K900091MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOROnufryk Low Vision Ent.K884360SEIKO P-6 PROGRESSIVE SPECTACLE LENSESSeiko Corp.K882814NEOLENS PRESCRIPTION SPECTACLE LENSNeolens, Inc.K882308CR-39 PLASTIC LENSES FOR EYEGLASSESAutomated Lens System

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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