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FDA 510(k)

SILCLAMPS DEGANIA SILICONE

K-Number: K920501 · 1992-06-02

ApplicantPuritas Health Care, Inc.
Decision Date1992-06-02
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SILCLAMPS DEGANIA SILICONE is the device name listed in this FDA 510(k) record. The listed applicant is Puritas Health Care, Inc.. It received FDA 510(k) clearance on 1992-06-02 under 510(k) number K920501. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILCLAMPS DEGANIA SILICONE?

SILCLAMPS DEGANIA SILICONE is a medical device that received FDA 510(k) clearance on 1992-06-02. The listed applicant is Puritas Health Care, Inc.. The 510(k) number is K920501.

When did SILCLAMPS DEGANIA SILICONE receive FDA 510(k) clearance?

SILCLAMPS DEGANIA SILICONE received FDA 510(k) clearance on 1992-06-02, under 510(k) number K920501.

Who is the listed applicant for SILCLAMPS DEGANIA SILICONE?

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

What is the FDA product code for SILCLAMPS DEGANIA SILICONE?

The FDA product code for SILCLAMPS DEGANIA SILICONE is DXC.

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Other records listing Puritas Health Care, 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.

K942339SKIN NEUVEAU SCAR TREATMENTK941197SILK*SKIN SCAR TREATMENTK935600TRACHEAL SUCTION CATHETERK935531OP-FLEX SUMP SUCTION SET WITH DIFFUSER TIPK940074Y-TYPE BLOOD ADMINISTRATION SETK940055MULTISET

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Related Devices (Code: DXC)

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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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