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FDA 510(k)

OBSTETRICAL KIT

K-Number: K822505 · 1982-09-30

ApplicantParr Emergency Product Sales, Inc.
Decision Date1982-09-30
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OBSTETRICAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Parr Emergency Product Sales, Inc.. It received FDA 510(k) clearance on 1982-09-30 under 510(k) number K822505. The device is classified under product code HHD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OBSTETRICAL KIT?

OBSTETRICAL KIT is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is Parr Emergency Product Sales, Inc.. The 510(k) number is K822505.

When did OBSTETRICAL KIT receive FDA 510(k) clearance?

OBSTETRICAL KIT received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822505.

Who is the listed applicant for OBSTETRICAL KIT?

The FDA 510(k) record lists Parr Emergency Product Sales, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OBSTETRICAL KIT?

The FDA product code for OBSTETRICAL KIT is HHD.

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.

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Related Devices (Code: HHD)

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.

K071827ALWAYS MENSTRUAL PADSProcter & Gamble, Inc.K012629ALWAYS DUETSProcter & Gamble Co.K003843ENVIVE MINIFORMSProcter & Gamble Co.K993870UNSCENTED INTERLABIAL MENSTRUAL PADProcter & Gamble Co.K980395GLADRAGS COTTON MENSTRUAL PADKeepers!, Inc.K953470FLUSHIES FLUSHABLE/BIODEGRADABLE MENSTRUAL PADS/NAPKINS (ULTRA THINS)Mediquip, Inc.

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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