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FDA 510(k)

BRENNEN MEDICAL STERILE SALINE SOLUTION

K-Number: K935060 · 1994-01-10

ApplicantBrennen Medical, Inc.
Decision Date1994-01-10
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BRENNEN MEDICAL STERILE SALINE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Brennen Medical, Inc.. It received FDA 510(k) clearance on 1994-01-10 under 510(k) number K935060. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRENNEN MEDICAL STERILE SALINE SOLUTION?

BRENNEN MEDICAL STERILE SALINE SOLUTION is a medical device that received FDA 510(k) clearance on 1994-01-10. The listed applicant is Brennen Medical, Inc.. The 510(k) number is K935060.

When did BRENNEN MEDICAL STERILE SALINE SOLUTION receive FDA 510(k) clearance?

BRENNEN MEDICAL STERILE SALINE SOLUTION received FDA 510(k) clearance on 1994-01-10, under 510(k) number K935060.

Who is the listed applicant for BRENNEN MEDICAL STERILE SALINE SOLUTION?

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

What is the FDA product code for BRENNEN MEDICAL STERILE SALINE SOLUTION?

The FDA product code for BRENNEN MEDICAL STERILE SALINE SOLUTION is KMF.

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Other records listing Brennen Medical, 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.

K050086BRENNEN MEDICAL SILVER GLUCAN WOUND DRESSINGK030460MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIXK021835BRENNEN MEDICAL SURGICAL MESH, GLUCAMESH/GLUCATEXK002078BETA GLUCAN GEL (MACROPRO GEL)K002077GLUCANPRO CREAMK000518MACROPRO GEL

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Related Devices (Code: KMF)

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, Inc.

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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