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FDA 510(k)

SAFE-TIPS EZ

K-Number: K951238 · 1995-05-23

ApplicantSafe Wave Products, Inc.
Decision Date1995-05-23
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SAFE-TIPS EZ is the device name listed in this FDA 510(k) record. The listed applicant is Safe Wave Products, Inc.. It received FDA 510(k) clearance on 1995-05-23 under 510(k) number K951238. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFE-TIPS EZ?

SAFE-TIPS EZ is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is Safe Wave Products, Inc.. The 510(k) number is K951238.

When did SAFE-TIPS EZ receive FDA 510(k) clearance?

SAFE-TIPS EZ received FDA 510(k) clearance on 1995-05-23, under 510(k) number K951238.

Who is the listed applicant for SAFE-TIPS EZ?

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

What is the FDA product code for SAFE-TIPS EZ?

The FDA product code for SAFE-TIPS EZ is EIA.

Related Devices (Code: EIA)

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.

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Official Source

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