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FDA 510(k)

SPAN-AID BRIDGING PILLOW SYSTEM

K-Number: K801518 · 1980-08-04

ApplicantSpan-America Medical Systems, Inc.
Decision Date1980-08-04
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPAN-AID BRIDGING PILLOW SYSTEM 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 1980-08-04 under 510(k) number K801518. The device is classified under product code HKX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPAN-AID BRIDGING PILLOW SYSTEM?

SPAN-AID BRIDGING PILLOW SYSTEM is a medical device that received FDA 510(k) clearance on 1980-08-04. The listed applicant is Span-America Medical Systems, Inc.. The 510(k) number is K801518.

When did SPAN-AID BRIDGING PILLOW SYSTEM receive FDA 510(k) clearance?

SPAN-AID BRIDGING PILLOW SYSTEM received FDA 510(k) clearance on 1980-08-04, under 510(k) number K801518.

Who is the listed applicant for SPAN-AID BRIDGING PILLOW SYSTEM?

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 SPAN-AID BRIDGING PILLOW SYSTEM?

The FDA product code for SPAN-AID BRIDGING PILLOW SYSTEM is HKX.

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

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Related Devices (Code: HKX)

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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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