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FDA 510(k)

TEST, ACID PHOSPHATASE

K-Number: K760161 · 1976-07-20

ApplicantPrinceton Biomedix
Decision Date1976-07-20
Product CodeCJR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TEST, ACID PHOSPHATASE is the device name listed in this FDA 510(k) record. The listed applicant is Princeton Biomedix. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760161. The device is classified under product code CJR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEST, ACID PHOSPHATASE?

TEST, ACID PHOSPHATASE is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Princeton Biomedix. The 510(k) number is K760161.

When did TEST, ACID PHOSPHATASE receive FDA 510(k) clearance?

TEST, ACID PHOSPHATASE received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760161.

Who is the listed applicant for TEST, ACID PHOSPHATASE?

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

What is the FDA product code for TEST, ACID PHOSPHATASE?

The FDA product code for TEST, ACID PHOSPHATASE is CJR.

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Other records listing Princeton Biomedix as applicant

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Related Devices (Code: CJR)

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.

K842516SANDARE ACID PHOSPHATASE PROCEDURESandare Chemical Co., 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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