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FDA 510(k)

DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN

K-Number: K800956 · 1980-10-03

Decision Date1980-10-03
Product CodeHED
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN 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 K800956. 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 DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN?

DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN 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 K800956.

When did DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN receive FDA 510(k) clearance?

DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN received FDA 510(k) clearance on 1980-10-03, under 510(k) number K800956.

Who is the listed applicant for DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN?

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 DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN?

The FDA product code for DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN is HED.

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 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.

View all 29 devices →

Related Devices (Code: HED)

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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