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FDA 510(k)

ORION STERILE OR TOWELS

K-Number: K903117 · 1990-12-31

ApplicantOrion Life Systems, Inc.
Decision Date1990-12-31
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ORION STERILE OR TOWELS is the device name listed in this FDA 510(k) record. The listed applicant is Orion Life Systems, Inc.. It received FDA 510(k) clearance on 1990-12-31 under 510(k) number K903117. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORION STERILE OR TOWELS?

ORION STERILE OR TOWELS is a medical device that received FDA 510(k) clearance on 1990-12-31. The listed applicant is Orion Life Systems, Inc.. The 510(k) number is K903117.

When did ORION STERILE OR TOWELS receive FDA 510(k) clearance?

ORION STERILE OR TOWELS received FDA 510(k) clearance on 1990-12-31, under 510(k) number K903117.

Who is the listed applicant for ORION STERILE OR TOWELS?

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

What is the FDA product code for ORION STERILE OR TOWELS?

The FDA product code for ORION STERILE OR TOWELS is KKX.

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Other records listing Orion Life Systems, Inc. as applicant

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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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