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FDA 510(k)

AMERICAN ALCOHOL PREP PAD STERILE MEDIUM

K-Number: K870718 · 1987-05-07

ApplicantSpan-America Medical Systems, Inc.
Decision Date1987-05-07
Product CodeLKB
DecisionSubstantially Equivalent

Device Summary

AMERICAN ALCOHOL PREP PAD STERILE MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Span-America Medical Systems, Inc.. It received FDA 510(k) clearance on 1987-05-07 under 510(k) number K870718. The device is classified under product code LKB. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMERICAN ALCOHOL PREP PAD STERILE MEDIUM?

AMERICAN ALCOHOL PREP PAD STERILE MEDIUM is a medical device that received FDA 510(k) clearance on 1987-05-07. The listed applicant is Span-America Medical Systems, Inc.. The 510(k) number is K870718.

When did AMERICAN ALCOHOL PREP PAD STERILE MEDIUM receive FDA 510(k) clearance?

AMERICAN ALCOHOL PREP PAD STERILE MEDIUM received FDA 510(k) clearance on 1987-05-07, under 510(k) number K870718.

Who is the listed applicant for AMERICAN ALCOHOL PREP PAD STERILE MEDIUM?

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

What is the FDA product code for AMERICAN ALCOHOL PREP PAD STERILE MEDIUM?

The FDA product code for AMERICAN ALCOHOL PREP PAD STERILE MEDIUM is LKB.

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Other records listing Span-America Medical Systems, Inc. as applicant

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Related Devices (Code: LKB)

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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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