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FDA 510(k)

EXETER LIP SEAL

K-Number: K790554 · 1979-04-10

Decision Date1979-04-10
Product CodeLFA
DecisionSubstantially Equivalent

Device Summary

EXETER LIP SEAL is the device name listed in this FDA 510(k) record. The listed applicant is Exeter Medical Labs, Inc.. It received FDA 510(k) clearance on 1979-04-10 under 510(k) number K790554. The device is classified under product code LFA. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXETER LIP SEAL?

EXETER LIP SEAL is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Exeter Medical Labs, Inc.. The 510(k) number is K790554.

When did EXETER LIP SEAL receive FDA 510(k) clearance?

EXETER LIP SEAL received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790554.

Who is the listed applicant for EXETER LIP SEAL?

The FDA 510(k) record lists Exeter Medical Labs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXETER LIP SEAL?

The FDA product code for EXETER LIP SEAL is LFA.

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.

Other records listing Exeter Medical Labs, Inc. as applicant

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: LFA)

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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