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FDA 510(k)

WALPEO TABLH

K-Number: K771202 · 1977-07-21

ApplicantWalpeo Corp.
Decision Date1977-07-21
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WALPEO TABLH is the device name listed in this FDA 510(k) record. The listed applicant is Walpeo Corp.. It received FDA 510(k) clearance on 1977-07-21 under 510(k) number K771202. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALPEO TABLH?

WALPEO TABLH is a medical device that received FDA 510(k) clearance on 1977-07-21. The listed applicant is Walpeo Corp.. The 510(k) number is K771202.

When did WALPEO TABLH receive FDA 510(k) clearance?

WALPEO TABLH received FDA 510(k) clearance on 1977-07-21, under 510(k) number K771202.

Who is the listed applicant for WALPEO TABLH?

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

What is the FDA product code for WALPEO TABLH?

The FDA product code for WALPEO TABLH is INQ.

Related Clinical Trials

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.

Related Devices (Code: INQ)

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.

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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