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FDA 510(k)

SAFETY HOLSTER, SINGLE-USE

K-Number: K790770 · 1979-05-18

ApplicantAspen Laboratories, Inc.
Decision Date1979-05-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SAFETY HOLSTER, SINGLE-USE is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1979-05-18 under 510(k) number K790770. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFETY HOLSTER, SINGLE-USE?

SAFETY HOLSTER, SINGLE-USE is a medical device that received FDA 510(k) clearance on 1979-05-18. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K790770.

When did SAFETY HOLSTER, SINGLE-USE receive FDA 510(k) clearance?

SAFETY HOLSTER, SINGLE-USE received FDA 510(k) clearance on 1979-05-18, under 510(k) number K790770.

Who is the listed applicant for SAFETY HOLSTER, SINGLE-USE?

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

What is the FDA product code for SAFETY HOLSTER, SINGLE-USE?

The FDA product code for SAFETY HOLSTER, SINGLE-USE is GEI.

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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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