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FDA 510(k)

SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED

K-Number: K921496 · 1992-08-14

Decision Date1992-08-14
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Alpine Specialties, Inc.. It received FDA 510(k) clearance on 1992-08-14 under 510(k) number K921496. The device is classified under product code CAT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED?

SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED is a medical device that received FDA 510(k) clearance on 1992-08-14. The listed applicant is Alpine Specialties, Inc.. The 510(k) number is K921496.

When did SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED receive FDA 510(k) clearance?

SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED received FDA 510(k) clearance on 1992-08-14, under 510(k) number K921496.

Who is the listed applicant for SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED?

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

What is the FDA product code for SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED?

The FDA product code for SKIN SAVER(TM) TUBING HOLDER, MODEL 1921 MODIFIED is CAT.

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 Alpine Specialties, 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.

Related Devices (Code: CAT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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