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FDA 510(k)

PARA CHECK (AKA EIGHT CHECK-C)

K-Number: K852992 · 1985-10-10

Decision Date1985-10-10
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PARA CHECK (AKA EIGHT CHECK-C) is the device name listed in this FDA 510(k) record. The listed applicant is Streck Laboratories, Inc.. It received FDA 510(k) clearance on 1985-10-10 under 510(k) number K852992. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARA CHECK (AKA EIGHT CHECK-C)?

PARA CHECK (AKA EIGHT CHECK-C) is a medical device that received FDA 510(k) clearance on 1985-10-10. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K852992.

When did PARA CHECK (AKA EIGHT CHECK-C) receive FDA 510(k) clearance?

PARA CHECK (AKA EIGHT CHECK-C) received FDA 510(k) clearance on 1985-10-10, under 510(k) number K852992.

Who is the listed applicant for PARA CHECK (AKA EIGHT CHECK-C)?

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

What is the FDA product code for PARA CHECK (AKA EIGHT CHECK-C)?

The FDA product code for PARA CHECK (AKA EIGHT CHECK-C) is JPK.

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.

Other records listing Streck Laboratories, 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.

View all 70 devices →

Related Devices (Code: JPK)

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.

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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