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FDA 510(k)

PFINGST PRESSURE PASTE

K-Number: K965026 · 1997-02-10

ApplicantPfingst & Co., Inc.
Decision Date1997-02-10
Product CodeEFH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PFINGST PRESSURE PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Pfingst & Co., Inc.. It received FDA 510(k) clearance on 1997-02-10 under 510(k) number K965026. The device is classified under product code EFH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PFINGST PRESSURE PASTE?

PFINGST PRESSURE PASTE is a medical device that received FDA 510(k) clearance on 1997-02-10. The listed applicant is Pfingst & Co., Inc.. The 510(k) number is K965026.

When did PFINGST PRESSURE PASTE receive FDA 510(k) clearance?

PFINGST PRESSURE PASTE received FDA 510(k) clearance on 1997-02-10, under 510(k) number K965026.

Who is the listed applicant for PFINGST PRESSURE PASTE?

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

What is the FDA product code for PFINGST PRESSURE PASTE?

The FDA product code for PFINGST PRESSURE PASTE is EFH.

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Related Devices (Code: EFH)

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.

K912632OCCLUDEPascal Co., Inc.K911259HYDENTPascal Co., Inc.K864572FIXTECTORProdent Intl., Inc.K870032REVISED T-SCAN SYSTEMSentek, Inc.K832647ARTICULATING PAPERArdent Intl., Inc.K833132MUCOSAL ADJUSTMENT PASTE LIQUID SPRAYMyo-Tronics Research, Inc.

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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