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FDA 510(k)

TULIP

K-Number: K970129 · 1997-08-18

ApplicantRichard Ting
Decision Date1997-08-18
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TULIP is the device name listed in this FDA 510(k) record. The listed applicant is Richard Ting. It received FDA 510(k) clearance on 1997-08-18 under 510(k) number K970129. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TULIP?

TULIP is a medical device that received FDA 510(k) clearance on 1997-08-18. The listed applicant is Richard Ting. The 510(k) number is K970129.

When did TULIP receive FDA 510(k) clearance?

TULIP received FDA 510(k) clearance on 1997-08-18, under 510(k) number K970129.

Who is the listed applicant for TULIP?

The FDA 510(k) record lists Richard Ting as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TULIP?

The FDA product code for TULIP is ELW.

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Related Devices (Code: ELW)

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

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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