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FDA 510(k)

DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641

K-Number: K962740 · 1996-09-06

Decision Date1996-09-06
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641 is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Flex Hospital Products, Inc.. It received FDA 510(k) clearance on 1996-09-06 under 510(k) number K962740. 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 DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641?

DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641 is a medical device that received FDA 510(k) clearance on 1996-09-06. The listed applicant is Medi-Flex Hospital Products, Inc.. The 510(k) number is K962740.

When did DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641 receive FDA 510(k) clearance?

DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641 received FDA 510(k) clearance on 1996-09-06, under 510(k) number K962740.

Who is the listed applicant for DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641?

The FDA 510(k) record lists Medi-Flex Hospital Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641?

The FDA product code for DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641 is KMF.

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.

Other records listing Medi-Flex Hospital Products, 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.

View all 13 devices →

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.

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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