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FDA 510(k)

RPPI STERILIZATION BAGS

K-Number: K934252 · 1994-06-17

ApplicantRoyal Precision Plastics, Inc.
Decision Date1994-06-17
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RPPI STERILIZATION BAGS is the device name listed in this FDA 510(k) record. The listed applicant is Royal Precision Plastics, Inc.. It received FDA 510(k) clearance on 1994-06-17 under 510(k) number K934252. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RPPI STERILIZATION BAGS?

RPPI STERILIZATION BAGS is a medical device that received FDA 510(k) clearance on 1994-06-17. The listed applicant is Royal Precision Plastics, Inc.. The 510(k) number is K934252.

When did RPPI STERILIZATION BAGS receive FDA 510(k) clearance?

RPPI STERILIZATION BAGS received FDA 510(k) clearance on 1994-06-17, under 510(k) number K934252.

Who is the listed applicant for RPPI STERILIZATION BAGS?

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

What is the FDA product code for RPPI STERILIZATION BAGS?

The FDA product code for RPPI STERILIZATION BAGS is KCT.

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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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