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FDA 510(k)

DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID

K-Number: K800954 · 1980-10-03

ApplicantThe Healthcare Group Laboratories, Inc.
Decision Date1980-10-03
Product CodeHED
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID is the device name listed in this FDA 510(k) record. The listed applicant is The Healthcare Group Laboratories, Inc.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K800954. The device is classified under product code HED. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID?

DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K800954.

When did DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID receive FDA 510(k) clearance?

DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID received FDA 510(k) clearance on 1980-10-03, under 510(k) number K800954.

Who is the listed applicant for DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID?

The FDA 510(k) record lists The Healthcare Group Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID?

The FDA product code for DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID is HED.

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Other records listing The Healthcare Group Laboratories, 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.

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Related Devices (Code: HED)

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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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