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FDA 510(k)

PEDERSON VAGINAL SPECULA

K-Number: K821291 · 1982-05-24

ApplicantConphar, Inc.
Decision Date1982-05-24
Product CodeHDF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PEDERSON VAGINAL SPECULA is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-05-24 under 510(k) number K821291. The device is classified under product code HDF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDERSON VAGINAL SPECULA?

PEDERSON VAGINAL SPECULA is a medical device that received FDA 510(k) clearance on 1982-05-24. The listed applicant is Conphar, Inc.. The 510(k) number is K821291.

When did PEDERSON VAGINAL SPECULA receive FDA 510(k) clearance?

PEDERSON VAGINAL SPECULA received FDA 510(k) clearance on 1982-05-24, under 510(k) number K821291.

Who is the listed applicant for PEDERSON VAGINAL SPECULA?

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

What is the FDA product code for PEDERSON VAGINAL SPECULA?

The FDA product code for PEDERSON VAGINAL SPECULA is HDF.

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Other records listing Conphar, 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.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

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Related Devices (Code: HDF)

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.

K926429VAGINAL SPECULA: CUSCO, GUTTMAN, INFANTThomasville Medical Assoc.K902019MODIFIED METAL SPECULUM & SPECIAL BULLET FORCEPSGynescope Corp.K891041MIYA SPECULUMZinnanti Surgical Instruments, Inc.K891044LASER SPECULAZinnanti Surgical Instruments, Inc.K890375VAGINAL SPECULUMKinetic Medical ProductsK862478HAYES VAGINAL SHIELDFranklin Medical USA, 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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