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FDA 510(k)

WET PACK

K-Number: K843783 · 1984-12-19

ApplicantE.M. Adams
Decision Date1984-12-19
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

WET PACK is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Adams. It received FDA 510(k) clearance on 1984-12-19 under 510(k) number K843783. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WET PACK?

WET PACK is a medical device that received FDA 510(k) clearance on 1984-12-19. The listed applicant is E.M. Adams. The 510(k) number is K843783.

When did WET PACK receive FDA 510(k) clearance?

WET PACK received FDA 510(k) clearance on 1984-12-19, under 510(k) number K843783.

Who is the listed applicant for WET PACK?

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

What is the FDA product code for WET PACK?

The FDA product code for WET PACK is EFQ.

Other records listing E.M. Adams 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.

View all 21 devices →

Related Devices (Code: EFQ)

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

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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