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FDA 510(k)

PAPER-PAK OB PADS

K-Number: K800952 · 1980-05-14

ApplicantPaper-Pak Products, Inc.
Decision Date1980-05-14
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PAPER-PAK OB PADS is the device name listed in this FDA 510(k) record. The listed applicant is Paper-Pak Products, Inc.. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K800952. 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 PAPER-PAK OB PADS?

PAPER-PAK OB PADS is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Paper-Pak Products, Inc.. The 510(k) number is K800952.

When did PAPER-PAK OB PADS receive FDA 510(k) clearance?

PAPER-PAK OB PADS received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800952.

Who is the listed applicant for PAPER-PAK OB PADS?

The FDA 510(k) record lists Paper-Pak Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAPER-PAK OB PADS?

The FDA product code for PAPER-PAK OB PADS 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Paper-Pak Products, 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.

K812232OBSTETRICAL PAD(STEAM STERILIZED)

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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